STEREOMED CAMERA
FDA 510(k) clearance K823534 · decided 1982-12-15
Clearance details
- K-number
- K823534
- Device name
- STEREOMED CAMERA
- Applicant
- Diseases of the Skin Clinic, P.A.
- Decision
- Substantially Equivalent
- Date received
- 1982-11-20
- Decision date
- 1982-12-15
- Days to decision
- 25 days
- Clearance type
- Traditional
- Product code
- FTT
- Device class
- 1
- Regulation number
- 878.4160
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.