Cleared Traditional

K800734 - RAPID FERMENTATION AGAR (RFA)

K800734 is an FDA 510(k) clearance for RAPID FERMENTATION AGAR (RFA), manufactured by Remel Co.. The device is a Class 1 Microbiology device with product code JSE cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K800734 · Remel Co. · Microbiology device
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May 1980
Decision
36d
Days
Class 1
Risk

K800734 is an FDA 510(k) clearance for the RAPID FERMENTATION AGAR (RFA). Classified as Culture Media, Multiple Biochemical Test (product code JSE), Class I - General Controls.

Submitted by Remel Co. (Mchenry, US). The FDA issued a Cleared decision on May 8, 1980 after a review of 36 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 Remel Co. devices

FDA 510(k) Submission Details - K800734

510(k) Number K800734 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 1980
Decision Date May 08, 1980
Days to Decision 36 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
66d faster than avg
Panel avg: 102d · This submission: 36d
Pathway characteristics
Predicate-based equivalence.

JSE Device Classification - Class 1, General Controls

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 43
Devices cleared under the same product code (JSE) and FDA review panel - the closest regulatory comparables to K800734.
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K791222 · Analytical Products, Inc. · Aug 1979