Cleared Traditional

K000012 - IMMULITE PHENOBARBITAL

K000012 is the FDA 510(k) clearance for IMMULITE PHENOBARBITAL by Diagnostic Products Corp.. It is a Class 2 Toxicology device (product code DLZ) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K000012 · Diagnostic Products Corp. · Toxicology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2000
Decision
60d
Days
Class 2
Risk

K000012 is an FDA 510(k) clearance for the IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5. Classified as Enzyme Immunoassay, Phenobarbital (product code DLZ), Class II - Special Controls.

Submitted by Diagnostic Products Corp. (Los Angeles, US). The FDA issued a Cleared decision on March 3, 2000 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3660 - the FDA toxicology device 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 K000012 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 03, 2000
Decision Date March 03, 2000
Days to Decision 60 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 87d · This submission: 60d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DLZ Enzyme Immunoassay, Phenobarbital
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3660
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 Toxicology devices follow this clearance model.

Regulatory Peers - DLZ Enzyme Immunoassay, Phenobarbital

All 28
Devices cleared under the same product code (DLZ) and FDA review panel - the closest regulatory comparables to K000012.
ONLINE PHENOBARBITAL, MODEL 03016757190 & 03510620
K071644 · Roche Diagnostics Corp. · Sep 2007
RANDOX PHENOBARBITAL
K011303 · Randox Laboratories, Ltd. · Jul 2001
EMIT 2000 PHENOBARBITAL ASSAY, MODEL OSR4D229
K011528 · Syva Co. · Jun 2001
ABBOTT AEROSET PHENOBARBITAL ASSEY AND CALIBRATORS
K993031 · Syva Co. · Jan 2000
VITROS CHEMISTRY PRODUCTS PHBR SLIDES
K984288 · Ortho-Clinical Diagnostics, Inc. · Jan 1999
PHENOBARBITAL ENZYME IMMUNOASSAY
K946210 · Diagnostic Reagents, Inc. · Feb 1995