UVATEC SUNTAMED 400
FDA 510(k) clearance K828670 · decided 1983-01-17
Clearance details
- K-number
- K828670
- Device name
- UVATEC SUNTAMED 400
- Applicant
- Solitec GmbH
- Decision
- Substantially Equivalent
- Date received
- 1982-11-30
- Decision date
- 1983-01-17
- Days to decision
- 48 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Planegg, DE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.