CHASE MR SYSTEM
K-Number: K072473 · 2007-12-10
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Device Summary
Frequently Asked Questions
What is the CHASE MR SYSTEM?
CHASE MR SYSTEM is a medical device that received FDA 510(k) clearance on 2007-12-10. The listed applicant is Chase Medical, LP. The 510(k) number is K072473.
When did CHASE MR SYSTEM receive FDA 510(k) clearance?
CHASE MR SYSTEM received FDA 510(k) clearance on 2007-12-10, under 510(k) number K072473.
Who is the listed applicant for CHASE MR SYSTEM?
The FDA 510(k) record lists Chase Medical, LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHASE MR SYSTEM?
The FDA product code for CHASE MR SYSTEM is LNH.
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 Chase Medical, LP 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: LNH)
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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