HISTOFREEZER
FDA 510(k) clearance K931299 · decided 1993-08-11
Clearance details
- K-number
- K931299
- Device name
- HISTOFREEZER
- Applicant
- Solarcare Technologies Corp,Inc.
- Decision
- Substantially Equivalent
- Date received
- 1993-03-15
- Decision date
- 1993-08-11
- Days to decision
- 149 days
- Clearance type
- Traditional
- Product code
- GEH
- Device class
- 2
- Regulation number
- 878.4350
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Bethlehem, PA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.