Cleared Traditional

K782039 - SERACON-N

K782039 is an FDA 510(k) clearance for SERACON-N, manufactured by Bhp Diagnostix, Inc.. The device is a Class 2 Chemistry device with product code JIX cleared through the Traditional 510(k) pathway after a 82-day FDA review.

K782039 · Bhp Diagnostix, Inc. · Chemistry device
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Feb 1979
Decision
82d
Days
Class 2
Risk

K782039 is an FDA 510(k) clearance for the SERACON-N. Classified as Calibrator, Multi-analyte Mixture (product code JIX), Class II - Special Controls.

Submitted by Bhp Diagnostix, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 26, 1979 after a review of 82 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - 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 Bhp Diagnostix, Inc. devices

FDA 510(k) Submission Details - K782039

510(k) Number K782039 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 06, 1978
Decision Date February 26, 1979
Days to Decision 82 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
6d faster than avg
Panel avg: 88d · This submission: 82d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JIX Device Classification - Class 2, Special Controls

Product Code JIX Calibrator, Multi-analyte Mixture
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
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 - JIX Calibrator, Multi-analyte Mixture

All 275
Devices cleared under the same product code (JIX) and FDA review panel - the closest regulatory comparables to K782039.
SERACON CAL D025
K791956 · Bhp Diagnostix, Inc. · Oct 1979
CALIBRATOR I
K791693 · Hi Chem, Inc. · Sep 1979
CALIBRATOR II
K791694 · Hi Chem, Inc. · Sep 1979
SERACON-A
K782037 · Bhp Diagnostix, Inc. · Feb 1979
SERACON-SRI
K781757 · Bhp Diagnostix, Inc. · Dec 1978
SERACON-SRII
K781758 · Bhp Diagnostix, Inc. · Dec 1978