510(k) K913883

COX DISPOSABLE BIOPSY FORCEP by Cox Medical Ent., Inc. — Product Code FCL

K913883 is an FDA 510(k) premarket notification submitted by Cox Medical Ent., Inc. for the device "COX DISPOSABLE BIOPSY FORCEP". The FDA issued a decision of Substantially Equivalent on October 5, 1991. The device falls under product code FCL (Forceps, Biopsy, Non-Electric), a Class I device regulated under 21 CFR 876.1075. Cox Medical Ent., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 5, 1991
Date Received
August 29, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, Biopsy, Non-Electric
Device Class
Class I
Regulation Number
876.1075
Review Panel
GU
Submission Type