BIOCIRCUITS IOS T4/TU TEST CARTRIDGES
K-Number: K952751 · 1995-11-20
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Device Summary
Frequently Asked Questions
What is the BIOCIRCUITS IOS T4/TU TEST CARTRIDGES?
BIOCIRCUITS IOS T4/TU TEST CARTRIDGES is a medical device that received FDA 510(k) clearance on 1995-11-20. The listed applicant is Biocircuits Corp.. The 510(k) number is K952751.
When did BIOCIRCUITS IOS T4/TU TEST CARTRIDGES receive FDA 510(k) clearance?
BIOCIRCUITS IOS T4/TU TEST CARTRIDGES received FDA 510(k) clearance on 1995-11-20, under 510(k) number K952751.
Who is the listed applicant for BIOCIRCUITS IOS T4/TU TEST CARTRIDGES?
The FDA 510(k) record lists Biocircuits Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOCIRCUITS IOS T4/TU TEST CARTRIDGES?
The FDA product code for BIOCIRCUITS IOS T4/TU TEST CARTRIDGES is KLI.
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 Biocircuits 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: KLI)
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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