Cleared Traditional

K973350 - BIO-RAD MICROPLATE 17-HYDROXYPROGESTERONE TEST

K973350 is an FDA 510(k) clearance for BIO-RAD MICROPLATE 17-HYDROXYPROGESTERO..., manufactured by Bio-Rad. The device is a Class 1 Chemistry device with product code JLX cleared through the Traditional 510(k) pathway after a 157-day FDA review.

K973350 · Bio-Rad · Chemistry device
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Feb 1998
Decision
157d
Days
Class 1
Risk

K973350 is an FDA 510(k) clearance for the BIO-RAD MICROPLATE 17-HYDROXYPROGESTERONE TEST. Classified as Radioimmunoassay, 17-hydroxyprogesterone (product code JLX), Class I - General Controls.

Submitted by Bio-Rad (Hercules, US). The FDA issued a Cleared decision on February 9, 1998 after a review of 157 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1395 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Bio-Rad devices

FDA 510(k) Submission Details - K973350

510(k) Number K973350 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 05, 1997
Decision Date February 09, 1998
Days to Decision 157 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
69d slower than avg
Panel avg: 88d · This submission: 157d
Pathway characteristics
Predicate-based equivalence.

JLX Device Classification - Class 1, General Controls

Product Code JLX Radioimmunoassay, 17-hydroxyprogesterone
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1395
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 - JLX Radioimmunoassay, 17-hydroxyprogesterone

All 10
Devices cleared under the same product code (JLX) and FDA review panel - the closest regulatory comparables to K973350.
MODIFICATION TO: AUTODELFIA NEONATAL 17A-OH-PROGESTERONE L KIT
K050960 · Wallac OY · Jul 2005
DELFIA NEONATAL 17A-OH-PROGESTERONE KIT
K042424 · Wallac OY · Sep 2004
AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
K042425 · Wallac OY · Sep 2004
ACCUSCREEN 17-HYDROXYPROGESTERONE
K934178 · Neometrics, Inc. · Mar 1995
DSL ACTIVE 17A-OH PROGESTERONE RIA (DSL 5000)
K943148 · Diagnostic Systems Laboratories, Inc. · Nov 1994
DSL 17A-OH PROGERSTERONE (DSL #6800)
K894265 · Diagnostic Systems Laboratories, Inc. · Sep 1989