SPECTRA (ULTRAVIOLET PRODUCTS)— 510(k) K827123
Substantially EquivalentUltralite
FDA 510(k) clearance K827123 for SPECTRA (ULTRAVIOLET PRODUCTS), Substantially Equivalent on 1982-03-05. Applicant: Ultralite.
Clearance details
- Applicant
- Ultralite
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wheatridge, CO, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.