Cleared Traditional

K841992 - MODIFICATION TO ACS CORONARY GUIDING

K841992 is the FDA 510(k) clearance for MODIFICATION TO ACS CORONARY GUIDING by Advanced Cardiovascular Systems, Inc.. It is a Class 2 Immunology device (product code DAO) cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K841992 · Advanced Cardiovascular Systems, Inc. · Immunology device
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Jun 1984
Decision
47d
Days
Class 2
Risk

K841992 is an FDA 510(k) clearance for the MODIFICATION TO ACS CORONARY GUIDING. Classified as Igm (mu Chain Specific), Antigen, Antiserum, Control (product code DAO), Class II - Special Controls.

Submitted by Advanced Cardiovascular Systems, Inc. (Santa Clara, US). The FDA issued a Cleared decision on June 11, 1984 after a review of 47 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5550 - the FDA immunology 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 Advanced Cardiovascular Systems, Inc. devices

Submission Details

510(k) Number K841992 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1984
Decision Date June 11, 1984
Days to Decision 47 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
57d faster than avg
Panel avg: 104d · This submission: 47d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DAO Igm (mu Chain Specific), Antigen, Antiserum, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5550
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 Immunology devices follow this clearance model.

Regulatory Peers - DAO Igm (mu Chain Specific), Antigen, Antiserum, Control

Devices cleared under the same product code (DAO) and FDA review panel - the closest regulatory comparables to K841992.
ROCHE DIAGNOSTICS TINA-QUANT IGM GEN.2
K040431 · Roche Diagnostics Corp. · Mar 2004
SPIFE URINE IFE
K982639 · Helena Laboratories · Nov 1998
BOEHRINGER MANNHEIM IGM ASSAY
K955908 · Boehringer Mannheim Corp. · Feb 1996
IMMUNOGL. FRCT. OF RABBIT ANTISER.-IGM
K812487 · Dako Corp. · Sep 1981
GEMENI IGM ASSAY
K800450 · Electro-Nucleonics Laboratories, Inc. · Apr 1980
ANTISERUM TO HUMAN IGM
K790705 · Kent Laboratories, Inc. · Apr 1979