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

CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSI

K Number: K926202 · Decision May 12, 1993
Classifications
1
FEI Numbers
292
Registration Numbers
292
Same Product Code
28
Applicant Total
11
Review Days
154

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Basic Information

Device Name
CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSI
K Number
K926202
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4022
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ndm Corp.
Date Received
December 9, 1992
Decision Date
May 12, 1993
Product Code
NAE
Advisory Committee
General, Plastic Surgery
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
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic

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Other Clearances by Ndm Corp.

K Number Device Name
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K853968 DIATEMP ELECTROSURGICAL PEN
K830663 PENCIL SKIN ABRADER
K810920 NDM DIATEMP INFANT ELECTROSURG. DISP. P.
K801158 NDM DIATEMP ELECTROSURGICAL DIS. PAD
K790730 NDM PAPER TAPE ECG ELECTRODE
K772354 I.V. CATHETER
K772160 ELECTROSURGICAL GROUNDING PAD
K761301 V-TRACE ECG BACKPAD
K760312 ELECTRODE, PNS
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