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

NYCOCARD U-ALBUMIN AND U-ALBUMIN CONTROL

K Number: K053553 · Decision Mar 9, 2006
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
36
Applicant Total
19
Review Days
79

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Basic Information

Device Name
NYCOCARD U-ALBUMIN AND U-ALBUMIN CONTROL
K Number
K053553
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5040
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Polymedco, Inc.
Date Received
December 20, 2005
Decision Date
March 9, 2006
Product Code
DCF
Advisory Committee
Immunology
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
DCF Albumin, Antigen, Antiserum, Control

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Other Clearances by Polymedco, Inc.

K Number Device Name
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K111143 POLY-CHEM 90 TOTAL BILIRUBIN
K100550 POLY-CHEM 90 DIRECT HDL CHOLESTEROL, POLY-CHEM 90 DIRECT LDL CHOLESTEROL, POLY-CHEM 90 CHOLESTEROL, POLY-CHEM 90 TRIGLYC
K090703 POLY-CHEM 90 GLUCOSE
K061944 POLY-CHEM CREATININE
K041408 POLYMEDCO OC AUTO MICRO 80 FOB TEST
K041297 POLYMEDCO OC LIGHT FOBT TEST
K033706 POLYMEDCO HOMOCYSTEINE TEST FOR THE POLY-CHEM AND HITACHI CHEMISTRY SYSTEMS
K023654 GLYCA-DIRECT FRUCTOSAMINE
Search all 19 clearances from Polymedco, Inc. →