510(k) K965146
K965146 is an FDA 510(k) premarket notification submitted by Axiom Medical, Inc. for the device "FLAT CLOSED WOUND DRAIN WITH TROCAR". The FDA issued a decision of Substantially Equivalent on March 10, 1997. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. Axiom Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 10, 1997
- Date Received
- December 23, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Irrigation
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type