BIOPSER— 510(k) K820519

Substantially Equivalent

Advanced Biomedical Instruments

FDA 510(k) clearance K820519 for BIOPSER, Substantially Equivalent on 1982-04-29. Applicant: Advanced Biomedical Instruments. Device class: 1.

Clearance details

Applicant: Advanced Biomedical Instruments
Product code: Code HFB
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1982-02-25
Decision date: 1982-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HFB

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 Advanced Biomedical Instruments

K843156 — BIOLAS YAG 100 CILAS, ERCELAS YAG 1001984-10-01
K842670 — BIOLAS YAG 1001984-08-08
K801197 — CO2 LASER1980-06-30

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