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

HEPARINIZED PENROSE TUBING

K Number: K760814 · Decision Nov 3, 1976
Classifications
1
FEI Numbers
190
Registration Numbers
190
Same Product Code
86
Applicant Total
62
Review Days
22

Basic Information

Device Name
HEPARINIZED PENROSE TUBING
K Number
K760814
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
SHERWOOD MEDICAL INDUSTRIES
Date Received
October 12, 1976
Decision Date
November 3, 1976
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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