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

HYDROGEL-PREP

K Number: K791726 · Decision Nov 20, 1979
Classifications
1
FEI Numbers
570
Registration Numbers
570
Same Product Code
87
Applicant Total
10
Review Days
77

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Basic Information

Device Name
HYDROGEL-PREP
K Number
K791726
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4014
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Spenco Medical Corp.
Date Received
September 4, 1979
Decision Date
November 20, 1979
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 Spenco Medical Corp.

K Number Device Name
K981902 SPENCO SILICONE GEL SHEET
K922228 2ND SKIN STERILE ADHESIVE STRIP
K911550 2ND SKIN MOIST BURN PADS WITH ALOE
K910927 SPENCIO SKIN GUARD KIT
K896533 SPENCO BREAST FORMS
K894898 2ND SKIN NON-STICK MOIST BURN PADS
K820906 SPENCO CRYOPRESS
K811184 SPENCO DERMAL PADS
K791162 GELSKIN