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FDA 510(k)

DAVIS+GECK REUSABLE TRTOCARS

K-Number: K930254 · 1994-03-24

ApplicantDavis & Geck, Inc.
Decision Date1994-03-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVIS+GECK REUSABLE TRTOCARS 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 1994-03-24 under 510(k) number K930254. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVIS+GECK REUSABLE TRTOCARS?

DAVIS+GECK REUSABLE TRTOCARS is a medical device that received FDA 510(k) clearance on 1994-03-24. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K930254.

When did DAVIS+GECK REUSABLE TRTOCARS receive FDA 510(k) clearance?

DAVIS+GECK REUSABLE TRTOCARS received FDA 510(k) clearance on 1994-03-24, under 510(k) number K930254.

Who is the listed applicant for DAVIS+GECK REUSABLE TRTOCARS?

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+GECK REUSABLE TRTOCARS?

The FDA product code for DAVIS+GECK REUSABLE TRTOCARS is GCJ.

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Related Devices (Code: GCJ)

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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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