510(k) K926586
K926586 is an FDA 510(k) premarket notification submitted by Look, Inc. for the device "REVISED LABELING FOR CHROMIC AND PLAIN GUT SUTURES". The FDA issued a decision of Substantially Equivalent on December 22, 1993. The device falls under product code GAL (Suture, Absorbable, Natural), a Class II device regulated under 21 CFR 878.4830. Look, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 22, 1993
- Date Received
- December 1, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Absorbable, Natural
- Device Class
- Class II
- Regulation Number
- 878.4830
- Review Panel
- SU
- Submission Type