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

COMBINE PAD OR ABD

K Number: K820105 · Decision Feb 5, 1982
Classifications
1
FEI Numbers
570
Registration Numbers
570
Same Product Code
87
Applicant Total
20
Review Days
21

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Basic Information

Device Name
COMBINE PAD OR ABD
K Number
K820105
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4014
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Stan-Pak Ent.
Date Received
January 15, 1982
Decision Date
February 5, 1982
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

Other 510(k) clearances with the same product code (NAB), ordered by most recent decision date.

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Other Clearances by Stan-Pak Ent.

K Number Device Name
K823058 DOSOMETRIC RELEASE STERILIZATION
K820100 FROSTED GLASS SLIDES
K820099 TRACH TAPE
K820140 WEBRIL CAST PADDING
K820108 TOPPER SPONGES
K820155 SPECIALIST CAST PADDING
K820106 X-RAY GUAZE SPONGES
K820107 GUAZE SPONGES, PLAIN
K820056 TELFA STRIPS
K820142 TUBULAR STOCKINETTE
Search all 20 clearances from Stan-Pak Ent. →