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FDA 510(k)

RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR

K-Number: K851440 · 1985-06-05

ApplicantSummit Industries, Inc.
Decision Date1985-06-05
Product CodeIXY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR 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 1985-06-05 under 510(k) number K851440. The device is classified under product code IXY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR?

RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR is a medical device that received FDA 510(k) clearance on 1985-06-05. The listed applicant is Summit Industries, Inc.. The 510(k) number is K851440.

When did RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR receive FDA 510(k) clearance?

RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR received FDA 510(k) clearance on 1985-06-05, under 510(k) number K851440.

Who is the listed applicant for RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR?

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 RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR?

The FDA product code for RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR is IXY.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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. B800K850198FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOGK850117XMA 325 (X-RAY GENERATOR)K850118XMA INTEGRATED TABLE

Related Devices (Code: IXY)

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.

K953336VRS 3 WALL STANDPhilips Medical Systems (Cleveland), Inc.K953402UNIVERSIX 190Philips Medical Systems (Cleveland), Inc.K946114SENSORI-MOTOR RATING SCALECmedK946260NTBS-1417, 1436, TBS-1417Scott Imaging Intl., Inc.K930230RADIOGRAPHIC WALL-MOUNTED CASSETTE HOLDERAmerican Medical Sales, Inc.K930249BC/WT/PFTingle X-Ray Products, 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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