BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI
K-Number: K944978 · 1995-05-03
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Device Summary
Frequently Asked Questions
What is the BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI?
BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI is a medical device that received FDA 510(k) clearance on 1995-05-03. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K944978.
When did BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI receive FDA 510(k) clearance?
BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI received FDA 510(k) clearance on 1995-05-03, under 510(k) number K944978.
Who is the listed applicant for BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI?
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 BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI?
The FDA product code for BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI is IZH.
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: IZH)
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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