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

CHOLESTEZYME-V EIKEN

K Number: K821105 · Decision May 5, 1982
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
229
Applicant Total
34
Review Days
15

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Basic Information

Device Name
CHOLESTEZYME-V EIKEN
K Number
K821105
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1175
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Syn-Kit, Inc.
Date Received
April 20, 1982
Decision Date
May 5, 1982
Product Code
CHH
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
CHH Enzymatic Esterase--Oxidase, Cholesterol

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CHH), ordered by most recent decision date.

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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. →