Cleared Traditional

K920293 - DAVIS AND GECK HANDHELD INST. STERILIZA...

K920293 is an FDA 510(k) clearance for DAVIS AND GECK HANDHELD INST. STERILIZA..., manufactured by Davis & Geck, Inc.. The device is a Class 2 General Hospital device with product code FLE cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K920293 · Davis & Geck, Inc. · General Hospital
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Apr 1992
Decision
90d
Days
Class 2
Risk

K920293 is an FDA 510(k) clearance for the DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY. Classified as Sterilizer, Steam (product code FLE), Class II - Special Controls.

Submitted by Davis & Geck, Inc. (Danbury, US). The FDA issued a Cleared decision on April 21, 1992 after a review of 90 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6880 - the FDA general hospital 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 General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Davis & Geck, Inc. devices

FDA 510(k) Submission Details - K920293

510(k) Number K920293 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 1992
Decision Date April 21, 1992
Days to Decision 90 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
39d faster than avg
Panel avg: 129d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FLE Device Classification - Class 2, Special Controls

Product Code FLE Sterilizer, Steam
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6880
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FLE Sterilizer, Steam

All 75
Devices cleared under the same product code (FLE) and FDA review panel - the closest regulatory comparables to K920293.
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K900432 · Midmark Corp. · Jul 1990
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K895848 · Scientific Device Laboratory, Inc. · Dec 1989