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

LIFESIGN MI MYOGLOBIN

K Number: K942052 · Decision Feb 7, 1995
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
45
Applicant Total
14
Review Days
285

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Basic Information

Device Name
LIFESIGN MI MYOGLOBIN
K Number
K942052
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5680
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Princeton Biomedix
Date Received
April 28, 1994
Decision Date
February 7, 1995
Product Code
DDR
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DDR Myoglobin, Antigen, Antiserum, Control

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K901011 BIOSIGN HCG-ONE STEP PREGNANCY TEST
K894705 BIOSPOT HCG-RAPID PREGNANCY TEST
K894750 BIOSTIX I. HCG - ONE STEP PREGNANCY TEST
K892654 BIOSTIX (TM)HCG--SIMPLE PREGNANCY TEST
K761315 ALKALINE PHOSPHATASE (ALP)/PNPP
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