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FDA 510(k)

FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG

K-Number: K850198 · 1985-05-14

ApplicantSummit Industries, Inc.
Decision Date1985-05-14
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG is the device name listed in this FDA 510(k) record. The listed applicant is Summit Industries, Inc.. It received FDA 510(k) clearance on 1985-05-14 under 510(k) number K850198. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG?

FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG is a medical device that received FDA 510(k) clearance on 1985-05-14. The listed applicant is Summit Industries, Inc.. The 510(k) number is K850198.

When did FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG receive FDA 510(k) clearance?

FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG received FDA 510(k) clearance on 1985-05-14, under 510(k) number K850198.

Who is the listed applicant for FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG?

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

What is the FDA product code for FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG?

The FDA product code for FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG is IYB.

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Other records listing Summit Industries, 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.

K874908C900 X-RAY FILM PROCESSORK874687COLLI-MATETM MODEL NO. B800K851440RDIOGRAPHIC WALL HOLDER OR FILM RECEPTORK850117XMA 325 (X-RAY GENERATOR)K850118XMA INTEGRATED TABLE

Related Devices (Code: IYB)

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.

K935123SUPERSTAND 300Wuestec Medical, Inc.K946261MTS-007, STS-008, SSMTS-010, EURO-40, 72, SUPER EURO 4072, 5000Scott Imaging Intl., Inc.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K940442MPR-814Xri, Inc.K935004MODEL ALPHA TS-2Dpa Consulting, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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