510(k) K831344
K831344 is an FDA 510(k) premarket notification submitted by Brimms, Inc. for the device "DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC". The FDA issued a decision of Substantially Equivalent on July 18, 1983. Brimms, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 18, 1983
- Date Received
- April 25, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No