Cleared Traditional

K792420 - SIM MEDIUM

K792420 is the FDA 510(k) clearance for SIM MEDIUM by Isle Media and Sterile Products, Inc.. It is a Class 1 Microbiology device (product code JSE) cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K792420 · Isle Media and Sterile Products, Inc. · Microbiology device
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Dec 1979
Decision
34d
Days
Class 1
Risk

K792420 is an FDA 510(k) clearance for the SIM MEDIUM. Classified as Culture Media, Multiple Biochemical Test (product code JSE), Class I - General Controls.

Submitted by Isle Media and Sterile Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 31, 1979 after a review of 34 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2320 - the FDA microbiology 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 Isle Media and Sterile Products, Inc. devices

Submission Details

510(k) Number K792420 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 27, 1979
Decision Date December 31, 1979
Days to Decision 34 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 102d · This submission: 34d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSE Culture Media, Multiple Biochemical Test
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2320
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 - JSE Culture Media, Multiple Biochemical Test

All 38
Devices cleared under the same product code (JSE) and FDA review panel - the closest regulatory comparables to K792420.
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K821592 · Hardy Media · Jul 1982
BCYE MEDIUM
K812911 · Gibco Laboratories Life Technologies, Inc. · Nov 1981
RAPID FERMENTATION AGAR (RFA)
K800734 · Remel Co. · May 1980
DECARBOXYLASE MOELLER BASE WITH OR WITH-
K792425 · Isle Media and Sterile Products, Inc. · Dec 1979
API 20E REAGENT QC
K791222 · Analytical Products, Inc. · Aug 1979
TRIPLE SUGAR IRON AGAR (TSI AGAR)
K791473 · Isle Media and Sterile Products, Inc. · Aug 1979