Apparatus, Electrosurgical
General, Plastic Surgery · 21 CFR 878.4400
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
