TISCHLER CERVICAL BIOPSY PUNCH FORCEPS— 510(k) K842112

Name: FDA 510(k) clearance K842112
Creator: U.S. Food and Drug Administration
Published: 1984-07-03

Substantially Equivalent

J. Sklar Mfg. Co., Inc.

FDA 510(k) clearance K842112 for TISCHLER CERVICAL BIOPSY PUNCH FORCEPS, Substantially Equivalent on 1984-07-03. Applicant: J. Sklar Mfg. Co., Inc.. Device class: 1.

Clearance details

Applicant: J. Sklar Mfg. Co., Inc.
Product code: Code HFB
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1984-05-29
Decision date: 1984-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HFB

view all

K011488 — SPIRABRUSH CX BIOPSY INSTRUMENT2002-02-22
K944444 — CIT BIOPSY PUNCHES1995-09-29
K930773 — SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS1994-07-28
K933767 — FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY1994-05-26
K926595 — OWENS BIOPSY FORCEPS1994-05-25

More clearances from J. Sklar Mfg. Co., Inc.

view all

K843693 — JACOBS HIGH VACUUM SUCTION UNIT 05-25701984-10-31
K842111 — KOGAN ENDOSPECULUM 9-1/21984-06-19
K822448 — SCISSORS, VARIOUS1982-09-14
K802457 — KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-66101981-01-12
K802458 — KEVORKIAN-YOUNGE BIOPSY CURETTE #90-66111981-01-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.