HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING
K-Number: K792169 · 1979-12-10
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Device Summary
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.
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
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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