Cleared Traditional

K921614 - MILENIA FOLIC ACID

K921614 is the FDA 510(k) clearance for MILENIA FOLIC ACID by Diagnostic Products Corp.. It is a Class 2 Chemistry device (product code CGN) cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K921614 · Diagnostic Products Corp. · Chemistry device
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Jun 1992
Decision
80d
Days
Class 2
Risk

K921614 is an FDA 510(k) clearance for the MILENIA FOLIC ACID. Classified as Acid, Folic, Radioimmunoassay (product code CGN), Class II - Special Controls.

Submitted by Diagnostic Products Corp. (Los Angeles, US). The FDA issued a Cleared decision on June 25, 1992 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1295 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Diagnostic Products Corp. devices

Submission Details

510(k) Number K921614 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 06, 1992
Decision Date June 25, 1992
Days to Decision 80 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
8d faster than avg
Panel avg: 88d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CGN Acid, Folic, Radioimmunoassay
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1295
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CGN Acid, Folic, Radioimmunoassay

All 45
Devices cleared under the same product code (CGN) and FDA review panel - the closest regulatory comparables to K921614.
RADIAS FOLATE ENZYME IMMUNOASSAY
K933571 · Bio-Rad · Oct 1993
STRATUS FOLATE FLUOROMETRIC ENZYME-LINKED ASSAY
K923286 · Baxter Diagnostics, Inc. · Sep 1992
ACCESS THEOPHYLLINE IMMUNOASSAY REAGENTS
K922823 · Bio-Rad Laboratories, Inc. · Aug 1992
CEDIA RED BLOOD CELL FOLATE REAGENT PACK
K921689 · Microgenics Corp. · Jun 1992
CIBA CORNING MAGIC LITE FOLATE IMMUNOASSAY
K893684 · Ciba Corning Diagnostics Corp. · Jul 1989
SOLID PHASE SIMUL TRAC VITAMIN B12
K822728 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Nov 1982