Cleared Traditional

K921583 - DRYSLIDE(TM)

K921583 is the FDA 510(k) clearance for DRYSLIDE(TM) by Difco Laboratories, Inc.. It is a Class 1 Microbiology device (product code JTO) cleared through the Traditional 510(k) pathway after a 102-day FDA review.

K921583 · Difco Laboratories, Inc. · Microbiology device
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Jun 1992
Decision
102d
Days
Class 1
Risk

K921583 is an FDA 510(k) clearance for the DRYSLIDE(TM), PYR. Classified as Discs, Strips And Reagents, Microorganism Differentiation (product code JTO), Class I - General Controls.

Submitted by Difco Laboratories, Inc. (Detroit, US). The FDA issued a Cleared decision on June 19, 1992 after a review of 102 days - within the typical 510(k) review window.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2660 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Difco Laboratories, Inc. devices

Submission Details

510(k) Number K921583 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 09, 1992
Decision Date June 19, 1992
Days to Decision 102 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
At panel average
Panel avg: 102d · This submission: 102d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JTO Discs, Strips And Reagents, Microorganism Differentiation
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2660
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 - JTO Discs, Strips And Reagents, Microorganism Differentiation

All 144
Devices cleared under the same product code (JTO) and FDA review panel - the closest regulatory comparables to K921583.
INDOXYL ACETATE DISK
K923700 · Remel Co. · Oct 1992
LAP DISK
K923827 · Remel Co. · Sep 1992
BACTIDROP INDOLE (ERLICH'S)
K920973 · Remel Co. · Jun 1992
BACTIDROP NINHYDRIN
K920971 · Remel Co. · May 1992
BACTIDROP PYR
K920972 · Remel Co. · May 1992
NIACIN CONTROL DISKS
K920257 · Remel Co. · Apr 1992