510(k) K903624
K903624 is an FDA 510(k) premarket notification submitted by Look, Inc. for the device "PLAIN AND CHROMIC GUT SUTURE". The FDA issued a decision of SN on September 18, 1990. 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
- SN ()
- Decision Date
- September 18, 1990
- Date Received
- August 8, 1990
- 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