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

POLYMEDCO HOMOCYSTEINE TEST FOR THE POLY-CHEM AND HITACHI CHEMISTRY SYSTEMS

K Number: K033706 · Decision Feb 4, 2004
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
28
Applicant Total
19
Review Days
70

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Basic Information

Device Name
POLYMEDCO HOMOCYSTEINE TEST FOR THE POLY-CHEM AND HITACHI CHEMISTRY SYSTEMS
K Number
K033706
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1377
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Polymedco, Inc.
Date Received
November 26, 2003
Decision Date
February 4, 2004
Product Code
LPS
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
LPS Urinary Homocystine (Nonquantitative) Test System

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Other Clearances by Polymedco, Inc.

K Number Device Name
K112408 POLY-CHEM 90 ISE MODULE
K110818 POLY-CHEM 90 ALBUMIN, BUN, CALCIUM, CARBON DIOXIDE, CREATININE, AND TOTAL PROTEIN TESTS
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
K053553 NYCOCARD U-ALBUMIN AND U-ALBUMIN CONTROL
K041408 POLYMEDCO OC AUTO MICRO 80 FOB TEST
K041297 POLYMEDCO OC LIGHT FOBT TEST
K023654 GLYCA-DIRECT FRUCTOSAMINE
Search all 19 clearances from Polymedco, Inc. →