510(k) K932385
K932385 is an FDA 510(k) premarket notification submitted by Rocket of London, Ltd. for the device "SUTURE REMOVING FORCEPS". The FDA issued a decision of Substantially Equivalent on August 6, 1993. The device falls under product code GEN (Forceps, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. Rocket of London, Ltd. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 6, 1993
- Date Received
- May 17, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Forceps, General & Plastic Surgery
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type