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

DEROYAL SURGICAL'S ENDOSCOPIC SPECIMEN RETRIEVAL POUCH

K Number: K942879 · Decision Jul 19, 1994
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
82
Review Days
32

Basic Information

Device Name
DEROYAL SURGICAL'S ENDOSCOPIC SPECIMEN RETRIEVAL POUCH
K Number
K942879
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DEROYAL INDUSTRIES, INC.
Date Received
June 17, 1994
Decision Date
July 19, 1994
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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