TAGO FIFFU-GEN, OROSOMUCOID
K-Number: K841734 · 1984-06-01
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Device Summary
Frequently Asked Questions
What is the TAGO FIFFU-GEN, OROSOMUCOID?
TAGO FIFFU-GEN, OROSOMUCOID is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is Tago, Inc.. The 510(k) number is K841734.
When did TAGO FIFFU-GEN, OROSOMUCOID receive FDA 510(k) clearance?
TAGO FIFFU-GEN, OROSOMUCOID received FDA 510(k) clearance on 1984-06-01, under 510(k) number K841734.
Who is the listed applicant for TAGO FIFFU-GEN, OROSOMUCOID?
The FDA 510(k) record lists Tago, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAGO FIFFU-GEN, OROSOMUCOID?
The FDA product code for TAGO FIFFU-GEN, OROSOMUCOID is LKL.
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 Tago, 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: LKL)
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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