Single Use Hot Biopsy Forceps FD-231— 510(k) K173495

Substantially Equivalent

Olympus Medical Systems Corp.

FDA 510(k) clearance K173495 for Single Use Hot Biopsy Forceps FD-231, Substantially Equivalent on 2018-11-30. Applicant: Olympus Medical Systems Corp.. Device class: 2.

Clearance details

Applicant
Olympus Medical Systems Corp.
Product code
Code QEC
Device class
Class 2
Regulation
21 CFR 876.4300
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Hachioji-Shi, JP
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