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FDA 510(k)

ALTAIREX BUCKY/CASSETTE TRAY COMBINATION

K-Number: K873849 · 1987-10-28

ApplicantAltairex Manufacturing, Inc.
Decision Date1987-10-28
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALTAIREX BUCKY/CASSETTE TRAY COMBINATION is the device name listed in this FDA 510(k) record. The listed applicant is Altairex Manufacturing, Inc.. It received FDA 510(k) clearance on 1987-10-28 under 510(k) number K873849. 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 ALTAIREX BUCKY/CASSETTE TRAY COMBINATION?

ALTAIREX BUCKY/CASSETTE TRAY COMBINATION is a medical device that received FDA 510(k) clearance on 1987-10-28. The listed applicant is Altairex Manufacturing, Inc.. The 510(k) number is K873849.

When did ALTAIREX BUCKY/CASSETTE TRAY COMBINATION receive FDA 510(k) clearance?

ALTAIREX BUCKY/CASSETTE TRAY COMBINATION received FDA 510(k) clearance on 1987-10-28, under 510(k) number K873849.

Who is the listed applicant for ALTAIREX BUCKY/CASSETTE TRAY COMBINATION?

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

What is the FDA product code for ALTAIREX BUCKY/CASSETTE TRAY COMBINATION?

The FDA product code for ALTAIREX BUCKY/CASSETTE TRAY COMBINATION is IXQ.

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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.K960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300Wuestec Medical, 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.

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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