DYNATRON 900
K-Number: K993919 · 2000-01-03
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Device Summary
Frequently Asked Questions
What is the DYNATRON 900?
DYNATRON 900 is a medical device that received FDA 510(k) clearance on 2000-01-03. The listed applicant is Dynatronics Corp.. The 510(k) number is K993919.
When did DYNATRON 900 receive FDA 510(k) clearance?
DYNATRON 900 received FDA 510(k) clearance on 2000-01-03, under 510(k) number K993919.
Who is the listed applicant for DYNATRON 900?
The FDA 510(k) record lists Dynatronics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNATRON 900?
The FDA product code for DYNATRON 900 is ITH.
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 Dynatronics Corp. 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: ITH)
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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