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

BRENNEN MEDICAL BETA GLUCAN CREAM, MACROPRO

K Number: K980962 · Decision Jul 29, 1998
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
144
Applicant Total
17
Review Days
135

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Basic Information

Device Name
BRENNEN MEDICAL BETA GLUCAN CREAM, MACROPRO
K Number
K980962
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Brennen Medical, Inc.
Date Received
March 16, 1998
Decision Date
July 29, 1998
Product Code
MGQ
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
MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic

Similar 510(k) Clearances

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

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Other Clearances by Brennen Medical, Inc.

K Number Device Name
K050086 BRENNEN MEDICAL SILVER GLUCAN WOUND DRESSING
K030460 MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
K021835 BRENNEN MEDICAL SURGICAL MESH, GLUCAMESH/GLUCATEX
K002078 BETA GLUCAN GEL (MACROPRO GEL)
K002077 GLUCANPRO CREAM
K000518 MACROPRO GEL
K000519 GLUCANPRO
K982825 BRENNEN MEDICAL BETA GLUCAN GEL
K982403 BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
K964241 BRENNEN MEDICAL GLUCAN II WOUND DRESSING
Search all 17 clearances from Brennen Medical, Inc. →