510(k) K926538

TISCHLER BIOPSY FORCEPS by Thomasville Medical Assoc. — Product Code HFB

K926538 is an FDA 510(k) premarket notification submitted by Thomasville Medical Assoc. for the device "TISCHLER BIOPSY FORCEPS". The FDA issued a decision of Substantially Equivalent on February 24, 1994. The device falls under product code HFB (Forceps, Biopsy, Gynecological), a Class I 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
December 30, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, Biopsy, Gynecological
Device Class
Class I
Regulation Number
884.4530
Review Panel
OB
Submission Type