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FDA 510(k)

TRAUMA TABLE

K-Number: K853535 · 1985-09-11

ApplicantXre Corp.
Decision Date1985-09-11
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRAUMA TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Xre Corp.. It received FDA 510(k) clearance on 1985-09-11 under 510(k) number K853535. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAUMA TABLE?

TRAUMA TABLE is a medical device that received FDA 510(k) clearance on 1985-09-11. The listed applicant is Xre Corp.. The 510(k) number is K853535.

When did TRAUMA TABLE receive FDA 510(k) clearance?

TRAUMA TABLE received FDA 510(k) clearance on 1985-09-11, under 510(k) number K853535.

Who is the listed applicant for TRAUMA TABLE?

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

What is the FDA product code for TRAUMA TABLE?

The FDA product code for TRAUMA TABLE is GDC.

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Other records listing Xre Corp. as applicant

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.

K973744UNICATH SP BI-PLANE (MODEL M269 & M289)K961193FULL FRAME ZOOM SYSTEMK960998XRE COLLIMATORK945449UNICATH LLU ANGIOGRAPHIC SYSTEMK936002CINEMAC QASK933460DVFX, MODEL M256

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Related Devices (Code: GDC)

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.

K971390QUANTUM 3080SP SURGICAL TABLESTERIS CorporationK970807MOBILE OPERATING TABLE 1132.01Stierlen-Maquet AGK964273DURA-BOARD ARMBOARDAllen Medical Systems, Inc.K940616SKYTRON ELITE 3500 TABLESkytron, Div. the Kmw Group, Inc.K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMidmark Corp.K914758MDT/SHAMPAINE MODEL 4900B SURGICAL TABLEMdt Corp., Inc.

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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