HARDYDISK, SULFA/TRIMETH
K-Number: K000271 · 2000-04-07
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Device Summary
Frequently Asked Questions
What is the HARDYDISK, SULFA/TRIMETH?
HARDYDISK, SULFA/TRIMETH is a medical device that received FDA 510(k) clearance on 2000-04-07. The listed applicant is Hardy Diagnostics. The 510(k) number is K000271.
When did HARDYDISK, SULFA/TRIMETH receive FDA 510(k) clearance?
HARDYDISK, SULFA/TRIMETH received FDA 510(k) clearance on 2000-04-07, under 510(k) number K000271.
Who is the listed applicant for HARDYDISK, SULFA/TRIMETH?
The FDA 510(k) record lists Hardy Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HARDYDISK, SULFA/TRIMETH?
The FDA product code for HARDYDISK, SULFA/TRIMETH is JTN.
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 Diagnostics 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: JTN)
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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