RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000
K-Number: K024342 · 2003-04-23
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Device Summary
Frequently Asked Questions
What is the RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000?
RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000 is a medical device that received FDA 510(k) clearance on 2003-04-23. The listed applicant is Daito Co., Ltd.. The 510(k) number is K024342.
When did RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000 receive FDA 510(k) clearance?
RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000 received FDA 510(k) clearance on 2003-04-23, under 510(k) number K024342.
Who is the listed applicant for RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000?
The FDA 510(k) record lists Daito Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000?
The FDA product code for RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000 is IXW.
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: IXW)
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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