Cleared Traditional

FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT (K792056) - FDA 510(k) Clearance

Class I Microbiology device.

K792056 · Fisher Scientific Co., LLC · Microbiology device
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Nov 1979
Decision
32d
Days
Class 1
Risk

K792056 is an FDA 510(k) clearance for the FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT. Classified as Culture Media, General Nutrient Broth (product code JSC), Class I - General Controls.

Submitted by Fisher Scientific Co., LLC (Mchenry, US). The FDA issued a Cleared decision on November 16, 1979 after a review of 32 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2350 - 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 Fisher Scientific Co., LLC devices

Submission Details

510(k) Number K792056 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 15, 1979
Decision Date November 16, 1979
Days to Decision 32 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
70d faster than avg
Panel avg: 102d · This submission: 32d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSC Culture Media, General Nutrient Broth
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2350
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 - JSC Culture Media, General Nutrient Broth

All 51
Devices cleared under the same product code (JSC) and FDA review panel - the closest regulatory comparables to K792056.
MINITEK GRAM-POSITIVE BROTH & SET AND
K822487 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1982
PEPTONE YEAST EXTRACT GLUCOSE BROTH
K803026 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Dec 1980
TRYPTIC SOY BROTH(TSB) W/C02 & 1% YEAST
K800426 · Abbott Laboratories · Mar 1980
TRYPTIC SOY BROTH W/C02,SPS&1% YEAST EXT
K800427 · Abbott Laboratories · Mar 1980
TRYPTIC SOY BROTH W/CYSTEINE AND
K800428 · Abbott Laboratories · Mar 1980
TRYPTIC SOY BROTH W/C02,CYSTEINE & 1%
K800429 · Abbott Laboratories · Mar 1980