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FDA 510(k)

MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300

K-Number: K960083 · 1996-07-24

ApplicantWuestec Medical, Inc.
Decision Date1996-07-24
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300 is the device name listed in this FDA 510(k) record. The listed applicant is Wuestec Medical, Inc.. It received FDA 510(k) clearance on 1996-07-24 under 510(k) number K960083. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300?

MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300 is a medical device that received FDA 510(k) clearance on 1996-07-24. The listed applicant is Wuestec Medical, Inc.. The 510(k) number is K960083.

When did MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300 receive FDA 510(k) clearance?

MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300 received FDA 510(k) clearance on 1996-07-24, under 510(k) number K960083.

Who is the listed applicant for MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300?

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

What is the FDA product code for MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300?

The FDA product code for MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300 is IXQ.

Related Clinical Trials

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.

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Other records listing Wuestec Medical, Inc. 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.

K993962PENSIL TRAUMA, MODEL WWS6100K992603XRT 600 R/F, WRF 0600K992103C-QUESTK981880DX-480, ADD ON DIGITAL IMAGERK974240LIGHTLINE-MK955414XRT 400

View all 9 devices →

Related Devices (Code: IXQ)

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.

K973842CARBON FIBER CONFORMAL COUCH TOPMedtec, Inc.K954225MED-TEC HAND GRIPMedtec, Inc.K946262EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLESScott Imaging Intl., Inc.K942916OCTOPAQUE UNIVERSALOctostop, Inc.K942190ID100 MOBILE FLUOROSCOPIC EXAMINING TABLEImage Diagnostics, Inc.K913425DIAL-A-RAD PORTA RAD TABLEDial-A-Rad

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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