FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DeRoyal Laprador Specimen Retrieval System

K Number: K171475 · Decision Aug 17, 2017
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
91
Review Days
90

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Basic Information

Device Name
DeRoyal Laprador Specimen Retrieval System
K Number
K171475
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Deroyal Industries, Inc.
Date Received
May 19, 2017
Decision Date
August 17, 2017
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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