FDA 510(k)
Substantially Equivalent
🇺🇸 United States
SPECTRA (ULTRAVIOLET PRODUCTS)
K Number: K827123
·
Decision Mar 5, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
6
Review Days
31
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- SPECTRA (ULTRAVIOLET PRODUCTS)
- K Number
- K827123
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Ultralite
- Date Received
- February 2, 1982
- Decision Date
- March 5, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- RA
- Third Party
- N
Other Clearances by Ultralite
| K Number | Device Name | ||
|---|---|---|---|
| K910091 | ULTRALITE PANELITE | May 30, 1991 | Substantially Equivalent |
| K861963 | ULTRALITE HF1236 HAND AND FOOT SYSTEM | Jun 25, 1986 | Substantially Equivalent |
| K820492 | SPECTRA305 | Mar 31, 1982 | Substantially Equivalent |
| K820280 | SPECTRA 305/350 | Mar 5, 1982 | Substantially Equivalent |
| K761179 | PSORALITE | May 3, 1977 | Substantially Equivalent |