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

ATAGO URINE SPECIFIC GRAVITY & SERUM

K Number: K842168 · Decision Jul 16, 1984
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
12
Applicant Total
11
Review Days
46

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Basic Information

Device Name
ATAGO URINE SPECIFIC GRAVITY & SERUM
K Number
K842168
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2800
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Kyoto Diagnostics, Inc.
Date Received
May 31, 1984
Decision Date
July 16, 1984
Product Code
JRE
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
JRE Refractometer For Clinical Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JRE), 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
K841715 KYOTEST UK URINE TEST REAGENT STRIP
K841713 KYOTEST UG URINE TEST REAGENT STRIP
K841714 KYOTEST 2V, URINE TEST REAGENT STRIP
K840828 KYOTEST 8V
K840827 KYOTEST 5V
K840996 URINE ANALYZER SYSTEM
K840829 KYOTEST UGK
Search all 11 clearances from Kyoto Diagnostics, Inc. →