RIT 113 FILM ANALYSIS SYSTEM
K-Number: K935928 · 1994-07-29
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Device Summary
Frequently Asked Questions
What is the RIT 113 FILM ANALYSIS SYSTEM?
RIT 113 FILM ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1994-07-29. The listed applicant is Radiological Imaging Technology, Inc.. The 510(k) number is K935928.
When did RIT 113 FILM ANALYSIS SYSTEM receive FDA 510(k) clearance?
RIT 113 FILM ANALYSIS SYSTEM received FDA 510(k) clearance on 1994-07-29, under 510(k) number K935928.
Who is the listed applicant for RIT 113 FILM ANALYSIS SYSTEM?
The FDA 510(k) record lists Radiological Imaging Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIT 113 FILM ANALYSIS SYSTEM?
The FDA product code for RIT 113 FILM ANALYSIS SYSTEM is IYE.
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 Radiological Imaging Technology, 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.
Related Devices (Code: IYE)
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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