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

KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)

K Number: K973507 · Decision Dec 15, 1997
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
66
Review Days
90

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Basic Information

Device Name
KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)
K Number
K973507
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
September 16, 1997
Decision Date
December 15, 1997
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

Similar 510(k) Clearances

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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
K973619 KENDALL CURITY NON-ADHERING DRESSING
K973509 KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING
K973546 KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER
K970266 KENDALL HYDROPHILIC POWDER WOUND DRESSING
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 →