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

SITE STRIP

K Number: K843200 · Decision Mar 12, 1985
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
3
Review Days
210

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Basic Information

Device Name
SITE STRIP
K Number
K843200
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4020
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
E-Med Corp.
Date Received
August 14, 1984
Decision Date
March 12, 1985
Product Code
NAD
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
NAD Dressing, Wound, Occlusive

Similar 510(k) Clearances

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Other Clearances by E-Med Corp.

K Number Device Name
K971619 MICROFUSE MEMBRANE INFUSION CATHETER
K792049 I.V. STRIP