Cleared Traditional

K831671 - MODIFIED SOYBEAN CASEIN DIGEST BROTH

K831671 is the FDA 510(k) clearance for MODIFIED SOYBEAN CASEIN DIGEST BROTH by Isle Media and Sterile Products, Inc.. It is a Class 1 Microbiology device (product code JSG) cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K831671 · Isle Media and Sterile Products, Inc. · Microbiology device
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Jul 1983
Decision
66d
Days
Class 1
Risk

K831671 is an FDA 510(k) clearance for the MODIFIED SOYBEAN CASEIN DIGEST BROTH. Classified as Culture Media, Non-selective And Non-differential (product code JSG), Class I - General Controls.

Submitted by Isle Media and Sterile Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 28, 1983 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2300 - 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 K831671 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 1983
Decision Date July 28, 1983
Days to Decision 66 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
36d faster than avg
Panel avg: 102d · This submission: 66d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSG Culture Media, Non-selective And Non-differential
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2300
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 - JSG Culture Media, Non-selective And Non-differential

All 175
Devices cleared under the same product code (JSG) and FDA review panel - the closest regulatory comparables to K831671.
BEEF EXTRACT
K833215 · Acumedia Manufacturers, Inc. · Oct 1983
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SHEEP BLOOD AGAR PLATE
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KNAI SODIUM POTASSIUM ANALYZER
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CONTACT PLATE LECITHIN & POLYSORBATE 80
K830063 · bioMerieux, Inc. · Feb 1983
NUTRIENT AGAR
K830068 · bioMerieux, Inc. · Feb 1983