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

UROPAPER EIKEN 7

K Number: K843754 · Decision Dec 18, 1984
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
80
Applicant Total
34
Review Days
84

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Basic Information

Device Name
UROPAPER EIKEN 7
K Number
K843754
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1340
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Syn-Kit, Inc.
Date Received
September 25, 1984
Decision Date
December 18, 1984
Product Code
JIL
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
JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JIL), 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
K843760 UROPAPER EIKEN G
K843756 UROPAPER EIKEN 5
K843759 UROPAPER EIKEN HAG
Search all 34 clearances from Syn-Kit, Inc. →