SURGICAL HAMMERS
FDA 510(k) clearance K802524 · decided 1980-11-12
Clearance details
- K-number
- K802524
- Device name
- SURGICAL HAMMERS
- Applicant
- Midshore Welding Corp.
- Decision
- Substantially Equivalent
- Date received
- 1980-10-16
- Decision date
- 1980-11-12
- Days to decision
- 27 days
- Clearance type
- Traditional
- Product code
- FZY
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.