PILLING WECK 2 PIECE TAKE-APART INSTRUMENTS— 510(k) K965176

Name: FDA 510(k) clearance K965176
Creator: U.S. Food and Drug Administration
Published: 1997-03-04

Substantially Equivalent

Pilling Weck Group

FDA 510(k) clearance K965176 for PILLING WECK 2 PIECE TAKE-APART INSTRUMENTS, Substantially Equivalent on 1997-03-04. Applicant: Pilling Weck Group. Device class: 2.

Clearance details

Applicant: Pilling Weck Group
Product code: Code OCZ
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1996-12-24
Decision date: 1997-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jeffrey, NH, US

Download summary PDF View on FDA.gov ↗

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