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

KTI TRANSPARENT WOUND DRESSING

K Number: K925660 · Decision Apr 20, 1993
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
79
Applicant Total
6
Review Days
161

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Basic Information

Device Name
KTI TRANSPARENT WOUND DRESSING
K Number
K925660
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kingston Technologies, Inc.
Date Received
November 10, 1992
Decision Date
April 20, 1993
Product Code
MGP
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
MGP Dressing, Wound And Burn, Occlusive

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Other Clearances by Kingston Technologies, Inc.

K Number Device Name
K935232 HYDROTORQUE GUIDE WIRE
K940814 HYDRO-M(TM) WOUND GEL
K940738 KTI HY-Q(TM) WOUND DRESSING
K921502 HYSORB WOUND DRESSING
K882157 PANAMEX(TM) URETERAL STENT