510(k) K852302
K852302 is an FDA 510(k) premarket notification submitted by Broadwest Corp. for the device "INOX IORCEPS JAR". The FDA issued a decision of Substantially Equivalent on July 2, 1985. Broadwest Corp. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 2, 1985
- Date Received
- May 29, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No