510(k) K940904
K940904 is an FDA 510(k) premarket notification submitted by Medical Insights, Inc. for the device "KITTNER DISSECTOR/PEANUT/CHERRY/STICK/TRIANGLE SPONGE/GAUZE ROSEBUD". The FDA issued a decision of Substantially Equivalent on April 14, 1994. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Medical Insights, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 14, 1994
- Date Received
- February 24, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Gauze/Sponge, Internal
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type