510(k) K925621
K925621 is an FDA 510(k) premarket notification submitted by Kirwan Surgical Products, Inc. for the device "IRRIGATION/ASPIRATION TUBING SET". The FDA issued a decision of Substantially Equivalent on May 7, 1993. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Kirwan Surgical Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 7, 1993
- Date Received
- November 6, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Aspiration And Injection, Disposable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type