DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR
K-Number: K954345 · 1995-10-18
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Device Summary
Frequently Asked Questions
What is the DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR?
DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1995-10-18. The listed applicant is Doosan Corp.. The 510(k) number is K954345.
When did DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR receive FDA 510(k) clearance?
DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR received FDA 510(k) clearance on 1995-10-18, under 510(k) number K954345.
Who is the listed applicant for DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR?
The FDA 510(k) record lists Doosan Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR?
The FDA product code for DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR 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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