THIO W/SUPPLEMENT
K-Number: K834321 · 1984-01-13
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Device Summary
Frequently Asked Questions
What is the THIO W/SUPPLEMENT?
THIO W/SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Hardy Media. The 510(k) number is K834321.
When did THIO W/SUPPLEMENT receive FDA 510(k) clearance?
THIO W/SUPPLEMENT received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834321.
Who is the listed applicant for THIO W/SUPPLEMENT?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THIO W/SUPPLEMENT?
The FDA product code for THIO W/SUPPLEMENT is JSG.
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 Hardy Media 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: JSG)
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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