KIT, RIA, HUMAN THYROID HORMONE
K-Number: K760044 · 1976-07-26
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Device Summary
Frequently Asked Questions
What is the KIT, RIA, HUMAN THYROID HORMONE?
KIT, RIA, HUMAN THYROID HORMONE is a medical device that received FDA 510(k) clearance on 1976-07-26. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K760044.
When did KIT, RIA, HUMAN THYROID HORMONE receive FDA 510(k) clearance?
KIT, RIA, HUMAN THYROID HORMONE received FDA 510(k) clearance on 1976-07-26, under 510(k) number K760044.
Who is the listed applicant for KIT, RIA, HUMAN THYROID HORMONE?
The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KIT, RIA, HUMAN THYROID HORMONE?
The FDA product code for KIT, RIA, HUMAN THYROID HORMONE is JLW.
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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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: JLW)
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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