Cleared Traditional

K921045 - DIASLIDE URINE CULTURING DEVICE

K921045 is an FDA 510(k) clearance for DIASLIDE URINE CULTURING DEVICE, manufactured by Savyon Diagnostics , Ltd.. The device is a Class 1 Microbiology device with product code JXA cleared through the Traditional 510(k) pathway after a 208-day FDA review.

K921045 · Savyon Diagnostics , Ltd. · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1992
Decision
208d
Days
Class 1
Risk

K921045 is an FDA 510(k) clearance for the DIASLIDE URINE CULTURING DEVICE. Classified as Kit, Screening, Urine (product code JXA), Class I - General Controls.

Submitted by Savyon Diagnostics , Ltd. (Ashdod, IL). The FDA issued a Cleared decision on September 28, 1992 after a review of 208 days - an extended review cycle.

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 Savyon Diagnostics , Ltd. devices

FDA 510(k) Submission Details - K921045

510(k) Number K921045 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 04, 1992
Decision Date September 28, 1992
Days to Decision 208 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
106d slower than avg
Panel avg: 102d · This submission: 208d
Pathway characteristics
Predicate-based equivalence.

JXA Device Classification - Class 1, General Controls

Product Code JXA Kit, Screening, Urine
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 - JXA Kit, Screening, Urine

All 13
Devices cleared under the same product code (JXA) and FDA review panel - the closest regulatory comparables to K921045.
URISCREEN
K981084 · Diatech Diagnostics,Inc. · Oct 1998
URINE SCREENING DEVICE
K972676 · Combact Diagnostic Systems , Ltd. · Feb 1998
BAC-T-SCREEN
K924218 · Biomerieux Vitek, Inc. · Feb 1993
GEN-PROBE PACE SYSTEM URINE SCREEN
K892216 · Gen-Probe, Inc. · Sep 1989
SLIDE CULTURE U 'EIKEN'
K861631 · Syn-Kit, Inc. · Jun 1986
URICHECK
K860905 · Difco Laboratories, Inc. · Apr 1986