DYNAMEQ-II OPTION
K-Number: K955466 · 1996-02-13
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Device Summary
Frequently Asked Questions
What is the DYNAMEQ-II OPTION?
DYNAMEQ-II OPTION is a medical device that received FDA 510(k) clearance on 1996-02-13. The listed applicant is Qualitone. The 510(k) number is K955466.
When did DYNAMEQ-II OPTION receive FDA 510(k) clearance?
DYNAMEQ-II OPTION received FDA 510(k) clearance on 1996-02-13, under 510(k) number K955466.
Who is the listed applicant for DYNAMEQ-II OPTION?
The FDA 510(k) record lists Qualitone as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNAMEQ-II OPTION?
The FDA product code for DYNAMEQ-II OPTION is ESD.
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 Qualitone 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: ESD)
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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