510(k) K842112

TISCHLER CERVICAL BIOPSY PUNCH FORCEPS by J. Sklar Mfg. Co., Inc. — Product Code HFB

K842112 is an FDA 510(k) premarket notification submitted by J. Sklar Mfg. Co., Inc. for the device "TISCHLER CERVICAL BIOPSY PUNCH FORCEPS". The FDA issued a decision of Substantially Equivalent on July 3, 1984. The device falls under product code HFB (Forceps, Biopsy, Gynecological), a Class I device regulated under 21 CFR 884.4530. J. Sklar Mfg. Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 3, 1984
Date Received
May 29, 1984
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