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

ACCESS DIGIWIPE SYSTEM

K Number: K853141 · Decision Nov 18, 1985
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
96
Applicant Total
9
Review Days
117

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Basic Information

Device Name
ACCESS DIGIWIPE SYSTEM
K Number
K853141
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6550
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Medtech Products, Inc.
Date Received
July 24, 1985
Decision Date
November 18, 1985
Product Code
KHE
Advisory Committee
Hematology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
KHE Reagent, Occult Blood

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K843601 ACCESS HEMAWIPE