510(k) K851782
K851782 is an FDA 510(k) premarket notification submitted by Artiberia for the device "25-450 TO 25-540 VARIOUS SUTURE FORCEPS". The FDA issued a decision of Substantially Equivalent on June 20, 1985. The device falls under product code GDL (Needle, Suturing, Reusable), a Class I device regulated under 21 CFR 878.4800. Artiberia has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 20, 1985
- Date Received
- April 25, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Suturing, Reusable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type