CASPER
K-Number: K953227 · 1995-11-22
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Device Summary
Frequently Asked Questions
What is the CASPER?
CASPER is a medical device that received FDA 510(k) clearance on 1995-11-22. The listed applicant is Northwest Medical Physics Center. The 510(k) number is K953227.
When did CASPER receive FDA 510(k) clearance?
CASPER received FDA 510(k) clearance on 1995-11-22, under 510(k) number K953227.
Who is the listed applicant for CASPER?
The FDA 510(k) record lists Northwest Medical Physics Center as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CASPER?
The FDA product code for CASPER is IXI.
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 Northwest Medical Physics Center 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: IXI)
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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