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

KYOTEST 5V

K Number: K840827 · Decision May 14, 1984
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
10
Applicant Total
11
Review Days
80

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Basic Information

Device Name
KYOTEST 5V
K Number
K840827
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1550
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Kyoto Diagnostics, Inc.
Date Received
February 24, 1984
Decision Date
May 14, 1984
Product Code
CEN
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
CEN Dye-Indicator, Ph (Urinary, Non-Quantitative)

Similar 510(k) Clearances

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

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Other Clearances by Kyoto Diagnostics, Inc.

K Number Device Name
K861733 ADDITIONAL KYOTEST URINE TEST REAGENT STRIPS
K843003 GLUCOSE AUTO& STAT GA-1120
K842750 OSMOTIC PRESSURE AUTO & STAT OM-6010
K842168 ATAGO URINE SPECIFIC GRAVITY & SERUM
K841715 KYOTEST UK URINE TEST REAGENT STRIP
K841713 KYOTEST UG URINE TEST REAGENT STRIP
K841714 KYOTEST 2V, URINE TEST REAGENT STRIP
K840828 KYOTEST 8V
K840996 URINE ANALYZER SYSTEM
K840829 KYOTEST UGK
Search all 11 clearances from Kyoto Diagnostics, Inc. →