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FDA 510(k)

HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING

K-Number: K792169 · 1979-12-10

Decision Date1979-12-10
Product CodeIZZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Corp.. It received FDA 510(k) clearance on 1979-12-10 under 510(k) number K792169. The device is classified under product code IZZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING?

HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING is a medical device that received FDA 510(k) clearance on 1979-12-10. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K792169.

When did HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING receive FDA 510(k) clearance?

HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING received FDA 510(k) clearance on 1979-12-10, under 510(k) number K792169.

Who is the listed applicant for HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING?

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

What is the FDA product code for HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING?

The FDA product code for HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING is IZZ.

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.

Other records listing Bennett X-Ray 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.

View all 23 devices →

Related Devices (Code: IZZ)

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.

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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