510(k) K841681
K841681 is an FDA 510(k) premarket notification submitted by Humi Corp. for the device "UTERINE MANIPULATOR 4.5MM". The FDA issued a decision of SESP on April 23, 1984. Humi Corp. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESP ()
- Decision Date
- April 23, 1984
- Date Received
- April 23, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No