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

MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR

K Number: K912750 · Decision Aug 2, 1991
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
38
Review Days
42

Basic Information

Device Name
MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR
K Number
K912750
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DEXIDE, INC.
Date Received
June 21, 1991
Decision Date
August 2, 1991
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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K953611 DEXIDE ENDO-LUBE KIT
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K924117 DEXIDE LAPAROSCOPIC KITS
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