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

INLET IRRIGATION/ASPIRATION VALVE AND PROBES

K Number: K923528 · Decision Jan 12, 1993
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
2
Review Days
180

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Basic Information

Device Name
INLET IRRIGATION/ASPIRATION VALVE AND PROBES
K Number
K923528
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Inlet Medical, Inc.
Date Received
July 16, 1992
Decision Date
January 12, 1993
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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Other Clearances by Inlet Medical, Inc.

K Number Device Name
K984600 METRA PS PROCEDURE KIT