Cleared Traditional

ISO-DATA 500 SERIES GAMMA COUNTER (K872430) - FDA 510(k) Clearance

Class I Toxicology device.

K872430 · Iso-Data, Inc. · Toxicology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1987
Decision
60d
Days
Class 1
Risk

K872430 is an FDA 510(k) clearance for the ISO-DATA 500 SERIES GAMMA COUNTER. Classified as Counter (beta, Gamma) For Clinical Use (product code JJJ), Class I - General Controls.

Submitted by Iso-Data, Inc. (Rolling Meadows, US). The FDA issued a Cleared decision on August 21, 1987 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.2320 - the FDA toxicology 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 Iso-Data, Inc. devices

Submission Details

510(k) Number K872430 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 22, 1987
Decision Date August 21, 1987
Days to Decision 60 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 87d · This submission: 60d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJJ Counter (beta, Gamma) For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2320
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 - JJJ Counter (beta, Gamma) For Clinical Use

All 13
Devices cleared under the same product code (JJJ) and FDA review panel - the closest regulatory comparables to K872430.
ABBOTT VERTEX ANALYZER
K920559 · Abbott Laboratories · Mar 1992
LS 5800 SERIES LIQUID SCINTILLATION
K813472 · Beckman Instruments, Inc. · Dec 1981
LIQUID SCINTILLATION SPECTROPHOTOMETER
K810345 · Beckman Instruments, Inc. · Feb 1981
PACE-4-AUTOMATIC RIA GAMMA-COUTER
K802578 · Philips Medical Systems (Cleveland), Inc. · Dec 1980
NUCLEAR SAMPLE READER
K790905 · Abbott Laboratories · Jun 1979
PRINTER
K772099 · Miles Laboratories, Inc. · Jan 1978