Device classification

Apparatus, Electrosurgical

General, Plastic Surgery · 21 CFR 878.4400

Class IIProduct code HAM
Open FDA's page for this record
Third party flag
Y
Life sustain support flag
N
Gmp exempt flag
N
Summary malfunction reporting
Eligible
Product code
HAM
Review panel
SU
Medical specialty
SU
Device name
Apparatus, Electrosurgical
Medical specialty description
General, Plastic Surgery
Device class
2
Regulation number
878.4400
Implant flag
N
Submission type ID
1
Harmonized identifiers (openFDA)
K number
K945861, K810014, K884174, K863091, K000079, K920100, K833648, K823755, K810015, K911353, K913300, K894663, K993306, K771186, K780293, K810920, K884175, K884173, K881334, K780118, K884171, K820664, K153472, K853291, K852184, K895337, K871435, K901248, K894762, K810909, K884172
Registration number
1526534, 3003898360, 1054241, 3003895930, 3007748817, 1315756, 1043214, 1219619, 2212018, 1061927, 3003955307, 1055236, 1526711, 1047843, 2245574, 3013421458, 1319660, 1836161, 3010041511, 1060680, 3013466775, 3011137372, 3012494290, 1319639, 1220477, 3013557562, 2184009, 3010220595, 1320894, 3004491689, 1643817, 1211998, 9617601, 3007305485, 8030607
FEI number
1526534, 3003898360, 3007748817, 1315756, 3011649541, 1043214, 1000136478, 1219619, 3000203000, 1000208624, 2212018, 3003955307, 1000112877, 1526711, 1047843, 2245574, 3002750084, 3013421458, 3006509795, 3010041511, 3013466775, 3001451571, 3012494290, 1000116158, 1220477, 3013557562, 3010220595, 1000112968, 3004491689, 1643817, 1000138054, 3002534070, 1211998, 3005747797, 3007305485
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.