510(k) K930110

MICRO SURGERY NEEDLE HOLDERS by Thomasville Medical Assoc. — Product Code KNA

K930110 is an FDA 510(k) premarket notification submitted by Thomasville Medical Assoc. for the device "MICRO SURGERY NEEDLE HOLDERS". The FDA issued a decision of Substantially Equivalent on February 24, 1994. The device falls under product code KNA (Instrument, Manual, Specialized Obstetric-Gynecologic), a Class II device regulated under 21 CFR 884.4530. Thomasville Medical Assoc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1994
Date Received
January 11, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Manual, Specialized Obstetric-Gynecologic
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type