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

BIOBRANE(R) II

K Number: K896110 · Decision Nov 28, 1989
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
9
Review Days
36

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BIOBRANE(R) II
K Number
K896110
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Sterling Drug, Inc.
Date Received
October 23, 1989
Decision Date
November 28, 1989
Product Code
KGN
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
KGN Wound Dressing With Animal-Derived Material(S)

Similar 510(k) Clearances

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

View all

Other Clearances by Sterling Drug, Inc.

K Number Device Name
K901369 GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE II
K875275 WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER
K840260 PERIOGRAF DURAPATITE 40-60 MESH
K820164 EMPTY STERILE CARPUJECT
K820023 CONAGRAF TM DURAPATITE CONES
K813257 ALVEOGRAF DURAPATITE(18-40 MESH)
K813070 PERIOGRAF
K780209 DILUTION SPIKE