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

GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN

K Number: K852986 · Decision Aug 19, 1985
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
12
Review Days
35

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Basic Information

Device Name
GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN
K Number
K852986
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Clinical Technology Corp.
Date Received
July 15, 1985
Decision Date
August 19, 1985
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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Other Clearances by Clinical Technology Corp.

K Number Device Name
K925080 TEK-LUBE
K872867 BIOSIGN
K880166 BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000
K872705 BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)
K855138 BOVIE ULTRASONIC SURGICAL SYSTEM
K854231 ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES
K853507 STERI-GRIP
K844565 BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT)
K841272 SICKLE-STAT HEMOGLOBIN S SCREEN KIT
K823077 URINARY BLADDER TEMP. SENSOR #81-003
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