FDA 510(k)

G.E. XT CEILING TUBE SUSPENSION

K-Number: K902980 · 1990-10-23

ApplicantElectromek Diagnostic Systems, Inc.

Decision Date1990-10-23

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

G.E. XT CEILING TUBE SUSPENSION is the device name listed in this FDA 510(k) record. The listed applicant is Electromek Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1990-10-23 under 510(k) number K902980. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.E. XT CEILING TUBE SUSPENSION?

G.E. XT CEILING TUBE SUSPENSION is a medical device that received FDA 510(k) clearance on 1990-10-23. The listed applicant is Electromek Diagnostic Systems, Inc.. The 510(k) number is K902980.

When did G.E. XT CEILING TUBE SUSPENSION receive FDA 510(k) clearance?

G.E. XT CEILING TUBE SUSPENSION received FDA 510(k) clearance on 1990-10-23, under 510(k) number K902980.

Who is the listed applicant for G.E. XT CEILING TUBE SUSPENSION?

The FDA 510(k) record lists Electromek Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for G.E. XT CEILING TUBE SUSPENSION?

The FDA product code for G.E. XT CEILING TUBE SUSPENSION is JAA.

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Other records listing Electromek Diagnostic Systems, Inc. as applicant

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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.