FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HDL-C EIKEN

K Number: K813192 · Decision Nov 27, 1981
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
79
Applicant Total
34
Review Days
10

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Basic Information

Device Name
HDL-C EIKEN
K Number
K813192
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Syn-Kit, Inc.
Date Received
November 17, 1981
Decision Date
November 27, 1981
Product Code
LBS
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
LBS Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl

Similar 510(k) Clearances

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Other Clearances by Syn-Kit, Inc.

K Number Device Name
K861098 SEROIDEN STREPTO KIT 'EIKEN'
K861631 SLIDE CULTURE U 'EIKEN'
K854819 CPR SLIDE EIKEN
K854820 RA 80 EIKEN
K853276 ASO SLIDE EIKEN
K843758 UROPAPER EIKEN GK
K843753 UROPAPER EIKEN GP
K843754 UROPAPER EIKEN 7
K843760 UROPAPER EIKEN G
K843756 UROPAPER EIKEN 5
Search all 34 clearances from Syn-Kit, Inc. →