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FDA 510(k)

RX PEDESTAL TABLE

K-Number: K772283 · 1977-12-15

ApplicantGeneral Electric Co.
Decision Date1977-12-15
Product CodeIZZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RX PEDESTAL TABLE is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1977-12-15 under 510(k) number K772283. The device is classified under product code IZZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RX PEDESTAL TABLE?

RX PEDESTAL TABLE is a medical device that received FDA 510(k) clearance on 1977-12-15. The listed applicant is General Electric Co.. The 510(k) number is K772283.

When did RX PEDESTAL TABLE receive FDA 510(k) clearance?

RX PEDESTAL TABLE received FDA 510(k) clearance on 1977-12-15, under 510(k) number K772283.

Who is the listed applicant for RX PEDESTAL TABLE?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RX PEDESTAL TABLE?

The FDA product code for RX PEDESTAL TABLE is IZZ.

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Related Devices (Code: IZZ)

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.

K971452MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLESiemens Medical Solutions USA, Inc.K952701MED-TRON SPECT IMAGING TABLEMed-Tron Products, Inc.K951315CATHETERIZATION TABLE KS-60Shimadzu Medical SystemsK951053ANGIOREX CAT-350BToshiba America Medical Systems, In.CK943926RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLEPhilips Medical Systems (Cleveland), Inc.K930273ALPHARaymax Medical Corp.

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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