9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS
FDA 510(k) clearance K851752 · decided 1985-06-20
Clearance details
- K-number
- K851752
- Device name
- 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS
- Applicant
- Artiberia
- Decision
- Substantially Equivalent
- Date received
- 1985-04-25
- Decision date
- 1985-06-20
- Days to decision
- 56 days
- Clearance type
- Traditional
- Product code
- GDN
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- San Antonio, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.