TRIODOTHYRONINE (TC) COATED TUBE RIA
K-Number: K926345 · 1993-02-25
Advertisement
Device Summary
Frequently Asked Questions
What is the TRIODOTHYRONINE (TC) COATED TUBE RIA?
TRIODOTHYRONINE (TC) COATED TUBE RIA is a medical device that received FDA 510(k) clearance on 1993-02-25. The listed applicant is Monobind. The 510(k) number is K926345.
When did TRIODOTHYRONINE (TC) COATED TUBE RIA receive FDA 510(k) clearance?
TRIODOTHYRONINE (TC) COATED TUBE RIA received FDA 510(k) clearance on 1993-02-25, under 510(k) number K926345.
Who is the listed applicant for TRIODOTHYRONINE (TC) COATED TUBE RIA?
The FDA 510(k) record lists Monobind as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIODOTHYRONINE (TC) COATED TUBE RIA?
The FDA product code for TRIODOTHYRONINE (TC) COATED TUBE RIA 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 Monobind 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.
Advertisement