T3 CLASP-BEAD EIA KIT
K-Number: K893620 · 1989-08-11
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Device Summary
Frequently Asked Questions
What is the T3 CLASP-BEAD EIA KIT?
T3 CLASP-BEAD EIA KIT is a medical device that received FDA 510(k) clearance on 1989-08-11. The listed applicant is Biotecx Laboratories, Inc.. The 510(k) number is K893620.
When did T3 CLASP-BEAD EIA KIT receive FDA 510(k) clearance?
T3 CLASP-BEAD EIA KIT received FDA 510(k) clearance on 1989-08-11, under 510(k) number K893620.
Who is the listed applicant for T3 CLASP-BEAD EIA KIT?
The FDA 510(k) record lists Biotecx Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T3 CLASP-BEAD EIA KIT?
The FDA product code for T3 CLASP-BEAD EIA KIT is CDP.
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 Biotecx Laboratories, Inc. 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: CDP)
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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