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

TARGET MICROALBUMINURIA TEST

K Number: K912246 · Decision Jul 19, 1991
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
37
Applicant Total
27
Review Days
59

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Basic Information

Device Name
TARGET MICROALBUMINURIA TEST
K Number
K912246
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1645
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Texas Immunology, Inc.
Date Received
May 21, 1991
Decision Date
July 19, 1991
Product Code
JIR
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
JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)

Similar 510(k) Clearances

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

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Other Clearances by Texas Immunology, Inc.

K Number Device Name
K991465 DRUG STOP
K980153 DRUG CHECK
K973208 FIRST SIGN
K972094 TARGET CARDIAC TROPONIN I TEST
K963680 TARGET MYOGLOBIN TEST
K910073 TARGET ASO TEST
K904105 V-TREND TARGET RF TEST
K892231 V-TREND TARGET CRP TEST
K890423 V-TREND TARGET CRP TEST
K890041 V-TREND TARGET IM TEST
Search all 27 clearances from Texas Immunology, Inc. →