FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BANDAGE, COMPRESSION, FISTULAID

K Number: K781110 · Decision Aug 18, 1978
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
30
Applicant Total
2
Review Days
46

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Basic Information

Device Name
BANDAGE, COMPRESSION, FISTULAID
K Number
K781110
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3610
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Medical Device Laboratories
Date Received
July 3, 1978
Decision Date
August 18, 1978
Product Code
DJC
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DJC Thin Layer Chromatography, Methamphetamine

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Other Clearances by Medical Device Laboratories

K Number Device Name
K771573 DUO-CATH FEMORAL