FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DERMASSIST TRANSPARENT SITE DRESSING

K Number: K924249 · Decision Feb 3, 1993
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
63
Applicant Total
12
Review Days
163

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Basic Information

Device Name
DERMASSIST TRANSPARENT SITE DRESSING
K Number
K924249
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5210
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wilshire Medical Products
Date Received
August 24, 1992
Decision Date
February 3, 1993
Product Code
KMK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KMK Device, Intravascular Catheter Securement

Similar 510(k) Clearances

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

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Other Clearances by Wilshire Medical Products

K Number Device Name
K946031 DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING
K946030 DERMASSIST(TM) HYDROGEL SATURATED GAUZE DRESSING
K944333 HYDRODERM GEL WOUND DRESSING
K941149 DERMAASSIST HYDROCOLLOID DRESSING
K941216 HYDRODERM EXTRA THIN INTELLIGENT HYDROCOLLIOID DRESSING
K941005 DERMASSIST(TM) XEROFORM PETROLATUM DRESSING
K940044 DERMASSIST WET DRESSING, SALINE
K936230 DERMASSIST PETROLATUM GAUZE,USP
K940076 DERMASSIST WET DRESSING, WATER
K936234 DERMASSIST OIL EMULSION NON-ADHERING WOUND DRESSING
Search all 12 clearances from Wilshire Medical Products →