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

C.S.R. WRAPPERS

K Number: K820689 · Decision Apr 9, 1982
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
15
Review Days
28

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Basic Information

Device Name
C.S.R. WRAPPERS
K Number
K820689
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
General Medical Co.
Date Received
March 12, 1982
Decision Date
April 9, 1982
Product Code
FRG
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
FRG Wrap, Sterilization

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K900110 OPERAND* LUBRICATING JELLY
K853635 SUBDERM TM
K844652 C.A.S.E. CONTAINER
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K820521 STERILIZATION WRAP
K802231 AIR VIVA II
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