510(k) K832147
K832147 is an FDA 510(k) premarket notification submitted by Brimfield Scientific Instruments for the device "CIRCUT 1". The FDA issued a decision of Substantially Equivalent on July 26, 1983. Brimfield Scientific Instruments has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 26, 1983
- Date Received
- June 30, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No