VARIVIEWER (X-RAY FILM VIEWER)
K-Number: K875233 · 1988-01-19
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Device Summary
Frequently Asked Questions
What is the VARIVIEWER (X-RAY FILM VIEWER)?
VARIVIEWER (X-RAY FILM VIEWER) is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Diversified Diagnostic Products, Inc.. The 510(k) number is K875233.
When did VARIVIEWER (X-RAY FILM VIEWER) receive FDA 510(k) clearance?
VARIVIEWER (X-RAY FILM VIEWER) received FDA 510(k) clearance on 1988-01-19, under 510(k) number K875233.
Who is the listed applicant for VARIVIEWER (X-RAY FILM VIEWER)?
The FDA 510(k) record lists Diversified Diagnostic Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VARIVIEWER (X-RAY FILM VIEWER)?
The FDA product code for VARIVIEWER (X-RAY FILM VIEWER) is IXC.
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.
Related Devices (Code: IXC)
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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