HDR MIAMI APPLICATOR
K-Number: K020176 · 2002-04-08
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Device Summary
Frequently Asked Questions
What is the HDR MIAMI APPLICATOR?
HDR MIAMI APPLICATOR is a medical device that received FDA 510(k) clearance on 2002-04-08. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K020176.
When did HDR MIAMI APPLICATOR receive FDA 510(k) clearance?
HDR MIAMI APPLICATOR received FDA 510(k) clearance on 2002-04-08, under 510(k) number K020176.
Who is the listed applicant for HDR MIAMI APPLICATOR?
The FDA 510(k) record lists Mick Radio-Nuclear Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HDR MIAMI APPLICATOR?
The FDA product code for HDR MIAMI APPLICATOR is JAQ.
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 Mick Radio-Nuclear Instruments, 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: JAQ)
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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