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

NON-STERILE FOLDED GAUZE

K Number: K780764 · Decision Jun 6, 1978
Classifications
1
FEI Numbers
570
Registration Numbers
570
Same Product Code
87
Applicant Total
14
Review Days
33

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Basic Information

Device Name
NON-STERILE FOLDED GAUZE
K Number
K780764
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4014
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
The Owenby Co.
Date Received
May 4, 1978
Decision Date
June 6, 1978
Product Code
NAB
Advisory Committee
General, Plastic Surgery
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
NAB Gauze / Sponge,Nonresorbable For External Use

Similar 510(k) Clearances

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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
K790210 STOCKINETTE, TUBULAR UNBLEACHED
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. →