Cleared Traditional

K061990 - DIMENSION VISTA MICROALBUMIN FLEX REAGE...

Also marketed or referenced as:
PROTEIN 3 CALIBRATOR PROTEIN 3 CONTROL

K061990 is the FDA 510(k) clearance for DIMENSION VISTA MICROALBUMIN FLEX REAGE... by Dade Behring, Inc.. It is a Class 2 Chemistry device (product code DCF) cleared through the Traditional 510(k) pathway after a 68-day FDA review.

K061990 · Dade Behring, Inc. · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2006
Decision
68d
Days
Class 2
Risk

K061990 is an FDA 510(k) clearance for the DIMENSION VISTA MICROALBUMIN FLEX REAGENT CARTRIDGE. Classified as Albumin, Antigen, Antiserum, Control (product code DCF), Class II - Special Controls.

Submitted by Dade Behring, Inc. (Newark, US). The FDA issued a Cleared decision on September 19, 2006 after a review of 68 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 866.5040 - 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 Dade Behring, Inc. devices

Submission Details

510(k) Number K061990 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 2006
Decision Date September 19, 2006
Days to Decision 68 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 88d · This submission: 68d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DCF Albumin, Antigen, Antiserum, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5040
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 - DCF Albumin, Antigen, Antiserum, Control

All 23
Devices cleared under the same product code (DCF) and FDA review panel - the closest regulatory comparables to K061990.
TINA-QUANT ALBUMIN GEN 2
K101203 · Roche Diagnostics · Sep 2010
COBAS 8000 MODULAR SERIES ANALYZER
K100853 · Roche Diagnostics Corp. · Sep 2010
SYNCHRON SYSTEMS MICROALBUMIN (MA) REAGENT, MODEL 475100
K082251 · Beckman Coulter, Inc. · Apr 2009
DCL MICROALBUMIN ASSAY, MODEL 252-20
K051191 · Diagnostic Chemicals , Ltd. · Jul 2005
VITROS CHEMISTRY PRODUCT MALB REAGENT, CALIBRATOR KIT 24, MALB PERFORMANCE VERIFIERS I AND II
K042643 · Ortho-Clinical Diagnostics, Inc. · Nov 2004
DIMENSION MICROALBUMIN (MALB) FLEX REAGENT CARTRIDGE METHOD, CALIBRATOR, MODELS DF114, DC114
K033525 · Dade Behring, Inc. · Jan 2004