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

CPR SLIDE EIKEN

K Number: K854819 · Decision Feb 26, 1986
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
69
Applicant Total
34
Review Days
85

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Basic Information

Device Name
CPR SLIDE EIKEN
K Number
K854819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Syn-Kit, Inc.
Date Received
December 3, 1985
Decision Date
February 26, 1986
Product Code
DCN
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DCN System, Test, C-Reactive Protein

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DCN), 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'
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
K843759 UROPAPER EIKEN HAG
Search all 34 clearances from Syn-Kit, Inc. →