Cleared Traditional

K894530 - FPR THEOPHYLLINE CALIBRATOR KIT

K894530 is an FDA 510(k) clearance for FPR THEOPHYLLINE CALIBRATOR KIT, manufactured by Colony Laboratories, Inc.. The device is a Class 2 Toxicology device with product code DLJ cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K894530 · Colony Laboratories, Inc. · Toxicology device
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Sep 1989
Decision
60d
Days
Class 2
Risk

K894530 is an FDA 510(k) clearance for the FPR THEOPHYLLINE CALIBRATOR KIT. Classified as Calibrators, Drug Specific (product code DLJ), Class II - Special Controls.

Submitted by Colony Laboratories, Inc. (Washington, US). The FDA issued a Cleared decision on September 18, 1989 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3200 - 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 Colony Laboratories, Inc. devices

FDA 510(k) Submission Details - K894530

510(k) Number K894530 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 1989
Decision Date September 18, 1989
Days to Decision 60 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
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.

DLJ Device Classification - Class 2, Special Controls

Product Code DLJ Calibrators, Drug Specific
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3200
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 - DLJ Calibrators, Drug Specific

All 111
Devices cleared under the same product code (DLJ) and FDA review panel - the closest regulatory comparables to K894530.
DUPONT ALCOHOL CALIBRATOR
K904308 · E.I. Dupont DE Nemours & Co., Inc. · Oct 1990
INNOFLUOR (TM) AMIKACIN CALIBRATOR SET
K903101 · Innotron of Oregon, Inc. · Aug 1990
INNOFLUOR DIGOXIN CALIBRATOR SET
K895826 · Innotron of Oregon, Inc. · Oct 1989
INNOFLUOR CARBAMAZEPINE CALIBRATOR SET
K893506 · Innotron of Oregon, Inc. · Aug 1989
INNOFLUOR(TM) QUINDINE CALIBATOR SET
K892212 · Innotron of Oregon, Inc. · Jun 1989
ACA VANCOMYCIN CALIBRATOR
K892901 · E.I. Dupont DE Nemours & Co., Inc. · May 1989