FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

BIOAQUACARE, MODEL C-10( VARIOUS SIZES) WITH AND WITHOUT GAUZE, BLISTER PACKAGED OR IN PLASTIC BAG CONTAINERS

K Number: K072068 · Decision Dec 21, 2007
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
2
Review Days
147

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Basic Information

Device Name
BIOAQUACARE, MODEL C-10( VARIOUS SIZES) WITH AND WITHOUT GAUZE, BLISTER PACKAGED OR IN PLASTIC BAG CONTAINERS
K Number
K072068
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bioartificial Gel Technologies (Bagtech), Inc.
Date Received
July 27, 2007
Decision Date
December 21, 2007
Product Code
FRO
Advisory Committee
Unknown
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
FRO Dressing, Wound, Drug

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Other Clearances by Bioartificial Gel Technologies (Bagtech), Inc.

K Number Device Name
K080471 RADIO BIOAQUACARE