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

BINAX EQUATE GLYCOHEMOGLOBIN

K Number: K874749 · Decision Aug 12, 1988
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
30
Review Days
268

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Basic Information

Device Name
BINAX EQUATE GLYCOHEMOGLOBIN
K Number
K874749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Binax, Inc.
Date Received
November 18, 1987
Decision Date
August 12, 1988
Product Code
LCP
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
LCP Assay, Glycosylated Hemoglobin

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K091489 CLEARVIEW ADVANCED STREP A , MODEL 737-430
K083744 BINAXNOW MALARIA POSITIVE CONTROL KIT, MODEL 665-010
K092223 MODIFICATION TO: BINAXNOW INFLUENZA A & B TEST
K080003 BINAXNOW G6PD TEST
K062109 BINAXNOW INFLUENZA A & B TEST
K053126 BINAXNOW INFLUENZA A & B TEST
K041049 BINAXNOW INFLUENZA A & B TEST
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