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

KENDALL HYDROPHILIC POWDER WOUND DRESSING

K Number: K970266 · Decision Apr 23, 1997
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
66
Review Days
90

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
KENDALL HYDROPHILIC POWDER WOUND DRESSING
K Number
K970266
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent for Some Indications
Applicant
Kendall Healthcare Products Co. Div.Of Tyco Health
Date Received
January 23, 1997
Decision Date
April 23, 1997
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 Kendall Healthcare Products Co. Div.Of Tyco Health

K Number Device Name
K973763 KENDALL CURITY IODOFORM PACKING STRIP
K973511 KENDALL CURITY PETROLATUM GAUZE
K973507 KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)
K973619 KENDALL CURITY NON-ADHERING DRESSING
K973509 KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING
K973546 KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER
K963446 KENDALL DUAL LUMEN CATHETER
K964899 KENDALL CURITY URETERAL CATHETER
K964519 CURITY THORACENTESIS TRAY
K961977 KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE
Search all 66 clearances from Kendall Healthcare Products Co. Div.Of Tyco Health →