SPIRABRUSH CX BIOPSY INSTRUMENT— 510(k) K011488

Substantially Equivalent

Trylon Corp.

FDA 510(k) clearance K011488 for SPIRABRUSH CX BIOPSY INSTRUMENT, Substantially Equivalent on 2002-02-22. Applicant: Trylon Corp.. Device class: 1.

Clearance details

Applicant: Trylon Corp.
Product code: Code HFB
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 2001-05-15
Decision date: 2002-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HFB

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K926595 — OWENS BIOPSY FORCEPS1994-05-25
K926527 — ROTO FIT BIOPSY FORCEPS1994-02-25

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