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

A/C ENZYMATIC HOMOCYSTEINE ASSAY

K Number: K030754 · Decision Jul 11, 2003
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
28
Applicant Total
3
Review Days
123

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Basic Information

Device Name
A/C ENZYMATIC HOMOCYSTEINE ASSAY
K Number
K030754
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1377
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Anticancer, Inc.
Date Received
March 10, 2003
Decision Date
July 11, 2003
Product Code
LPS
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
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

Similar 510(k) Clearances

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

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Other Clearances by Anticancer, Inc.

K Number Device Name
K111260 A/C ENZYMATIC VITAMIN B6 ASSAY
K080851 A/C PORTABLE ENZYMATIC HOMOCYSTEINE ASSAY