FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

STOCKINETTE, TUBULAR UNBLEACHED

K Number: K790210 · Decision Feb 27, 1979
Classifications
1
FEI Numbers
681
Registration Numbers
681
Same Product Code
41
Applicant Total
14
Review Days
28

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Basic Information

Device Name
STOCKINETTE, TUBULAR UNBLEACHED
K Number
K790210
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5075
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
The Owenby Co.
Date Received
January 30, 1979
Decision Date
February 27, 1979
Product Code
FQM
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
FQM Bandage, Elastic

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Other Clearances by The Owenby Co.

K Number Device Name
K801628 RESTRAINT, PROTECTIVE
K801627 COVER, LIMB
K801532 STOCKINETTE, STERILE TWO PLY W/PULL TABS
K801626 ARM SLING
K801531 ARM SLING
K780764 NON-STERILE FOLDED GAUZE
K780418 BURN DRESSING PAD
K770889 BURN DRESSING KIT
K761069 P.S.M. BOTIQUE CAP
K761068 P.S.M. BOUFFANT CAP
Search all 14 clearances from The Owenby Co. →