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FDA 510(k)

DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY

K-Number: K920293 · 1992-04-21

ApplicantDavis & Geck, Inc.
Decision Date1992-04-21
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1992-04-21 under 510(k) number K920293. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY?

DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K920293.

When did DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY receive FDA 510(k) clearance?

DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY received FDA 510(k) clearance on 1992-04-21, under 510(k) number K920293.

Who is the listed applicant for DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY?

The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY?

The FDA product code for DAVIS AND GECK HANDHELD INST. STERILIZATION TRAY is FLE.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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