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

HYDRON BURN DRESSING FIELD KIT

K Number: K791865 · Decision Nov 16, 1979
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
34
Review Days
56

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Basic Information

Device Name
HYDRON BURN DRESSING FIELD KIT
K Number
K791865
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
National Patent Development Corp.
Date Received
September 21, 1979
Decision Date
November 16, 1979
Product Code
KMF
Advisory Committee
General Hospital
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
KMF Bandage, Liquid

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K Number Device Name
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K820028 ZEON COMPOSITE RESIN LIGHT CURE SYS
K820006 ZEON COMPOSITE RESIN SYSTEM
K811446 HYDRON WOUND DRESSING KIT
K801483 MARK IV SYRINGE
K801484 ROOT CANAL FILLING APPLICATOR NEEDLES
K801482 HYDRON ROOT CANAL FILLING MATERIAL
K792136 HYPO-ALLERGENIC PLASTIC TAPE
Search all 34 clearances from National Patent Development Corp. →