Cleared Traditional

K861997 - PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE

K861997 is the FDA 510(k) clearance for PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE by Hazleton Research Products, Inc.. It is a Class 1 Microbiology device (product code JSK) cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K861997 · Hazleton Research Products, Inc. · Microbiology device
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Jun 1986
Decision
18d
Days
Class 1
Risk

K861997 is an FDA 510(k) clearance for the PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE. Classified as Supplement, Culture Media (product code JSK), Class I - General Controls.

Submitted by Hazleton Research Products, Inc. (Denver, US). The FDA issued a Cleared decision on June 10, 1986 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2450 - 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 Hazleton Research Products, Inc. devices

Submission Details

510(k) Number K861997 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 1986
Decision Date June 10, 1986
Days to Decision 18 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
84d faster than avg
Panel avg: 102d · This submission: 18d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSK Supplement, Culture Media
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2450
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 - JSK Supplement, Culture Media

All 56
Devices cleared under the same product code (JSK) and FDA review panel - the closest regulatory comparables to K861997.
HEMOGLOBIN POWDER
K881566 · Acumedia Manufacturers, Inc. · Apr 1988
PENICILLIN-STREPTOMYCIN-FUNGIZONE
K861791 · Flow Laboratories, Inc. · May 1986
GENTAMICIN SULFATE SOLUTION (50MG GENTAMICIN)
K861823 · Flow Laboratories, Inc. · May 1986
GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)
K861824 · Flow Laboratories, Inc. · May 1986
ABBOTT CATION SUPPLEMENT SOLUTION
K853546 · Abbott Laboratories · Sep 1985
PRESTON CAMPYLOBACTER SELECTIVE SUPP
K840330 · Oxoid U.S.A., Inc. · May 1984