SPECTRA (ULTRAVIOLET PRODUCTS)
FDA 510(k) clearance K827123 · decided 1982-03-05
Clearance details
- K-number
- K827123
- Device name
- SPECTRA (ULTRAVIOLET PRODUCTS)
- Applicant
- Ultralite
- Decision
- Substantially Equivalent
- Date received
- 1982-02-02
- Decision date
- 1982-03-05
- Days to decision
- 31 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Wheatridge, CO, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.