Cleared Traditional

K871339 - KALLESTAD QM300 PROTEIN ANALYSIS SYSTEM

K871339 is the FDA 510(k) clearance for KALLESTAD QM300 PROTEIN ANALYSIS SYSTEM by Kallestad Diag, A Div. of Erbamont, Inc.. It is a Class 1 Immunology device (product code JQP) cleared through the Traditional 510(k) pathway after a 43-day FDA review.

K871339 · Kallestad Diag, A Div. of Erbamont, Inc. · Immunology device
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May 1987
Decision
43d
Days
Class 1
Risk

K871339 is an FDA 510(k) clearance for the KALLESTAD QM300 PROTEIN ANALYSIS SYSTEM. Classified as Calculator/data Processing Module, For Clinical Use (product code JQP), Class I - General Controls.

Submitted by Kallestad Diag, A Div. of Erbamont, Inc. (Chaska, US). The FDA issued a Cleared decision on May 15, 1987 after a review of 43 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 862.2100 - 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 Kallestad Diag, A Div. of Erbamont, Inc. devices

Submission Details

510(k) Number K871339 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 1987
Decision Date May 15, 1987
Days to Decision 43 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
61d faster than avg
Panel avg: 104d · This submission: 43d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JQP Calculator/data Processing Module, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2100
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JQP Calculator/data Processing Module, For Clinical Use

All 48
Devices cleared under the same product code (JQP) and FDA review panel - the closest regulatory comparables to K871339.
MODIFIED MODEL 570 CLINICAL CHEMISTRY ANALYZER
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COBAS MFC
K885292 · Roche Diagnostic Systems, Inc. · Mar 1989
710 PLUS
K864557 · Ciba Corning Diagnostics Corp. · Feb 1987
GLUCOFACTS DATA MANAGEMENT SYSTEM
K861844 · Miles Laboratories, Inc. · Aug 1986
GLUCOFACTS DATA PRINTER
K861779 · Miles Laboratories, Inc. · Aug 1986