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

HEMOCARD, HEMOGLOBIN C ASSAY

K Number: K923153 · Decision Jan 27, 1994
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
0
Applicant Total
44
Review Days
577

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Basic Information

Device Name
HEMOCARD, HEMOGLOBIN C ASSAY
K Number
K923153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7415
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Isolab, Inc.
Date Received
June 29, 1992
Decision Date
January 27, 1994
Product Code
MLL
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
MLL Hemoglobin C (Abnormal Hemoglobin Variant)

Other Clearances by Isolab, Inc.

K Number Device Name
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K950803 ISOLAB'S GALACTOSE-1-PHOSPHATE URIDYL TRANFERASE TEST KITS 800, 4000 SAMPLE
K950415 FLUOROSCAN NEONATAL
K942276 QUIK-SEP QUANTITATIVE HEMOGLOBIN S ASSAY
K942222 QUIK-SEP QUANTITIVE HEMOGLOBIN S CONTROLS
K944185 ISOSCAN
K934013 RESOLVE SYSTEMS ALKALINE PHOSPHATASE TEST KIT
K931234 HEMOCARD CONTROL HB-AA, AE, FAA, FAE
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