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FDA 510(k)

G.E. 48-4 CEILING TUBEHANGER

K-Number: K902791 · 1990-10-29

ApplicantElectromek Diagnostic Systems, Inc.
Decision Date1990-10-29
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

G.E. 48-4 CEILING TUBEHANGER 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 1990-10-29 under 510(k) number K902791. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.E. 48-4 CEILING TUBEHANGER?

G.E. 48-4 CEILING TUBEHANGER is a medical device that received FDA 510(k) clearance on 1990-10-29. The listed applicant is Electromek Diagnostic Systems, Inc.. The 510(k) number is K902791.

When did G.E. 48-4 CEILING TUBEHANGER receive FDA 510(k) clearance?

G.E. 48-4 CEILING TUBEHANGER received FDA 510(k) clearance on 1990-10-29, under 510(k) number K902791.

Who is the listed applicant for G.E. 48-4 CEILING TUBEHANGER?

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. 48-4 CEILING TUBEHANGER?

The FDA product code for G.E. 48-4 CEILING TUBEHANGER is KPR.

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Other records listing Electromek Diagnostic Systems, Inc. as applicant

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Related Devices (Code: KPR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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