510(k) K915406
K915406 is an FDA 510(k) premarket notification submitted by Davol, Inc. for the device "DAVOL ELECTROSUGICAL PROBES". The FDA issued a decision of Substantially Equivalent on February 28, 1992. The device falls under product code HFG (Coagulator, Laparoscopic, Unipolar (And Accessories)), a Class II device regulated under 21 CFR 884.4160. Davol, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 28, 1992
- Date Received
- December 2, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Coagulator, Laparoscopic, Unipolar (And Accessories)
- Device Class
- Class II
- Regulation Number
- 884.4160
- Review Panel
- OB
- Submission Type