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

STRYKER STRYKEFLOW SUCTION IRRIGATOR (MODIFICATION)

K Number: K954726 · Decision Nov 29, 1995
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
86
Applicant Total
101
Review Days
118

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Basic Information

Device Name
STRYKER STRYKEFLOW SUCTION IRRIGATOR (MODIFICATION)
K Number
K954726
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
August 3, 1995
Decision Date
November 29, 1995
Product Code
GCX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

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