TB KINYOUN CARBOLFUCHSIN
K-Number: K872187 · 1987-07-29
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Device Summary
Frequently Asked Questions
What is the TB KINYOUN CARBOLFUCHSIN?
TB KINYOUN CARBOLFUCHSIN is a medical device that received FDA 510(k) clearance on 1987-07-29. The listed applicant is Remel Co.. The 510(k) number is K872187.
When did TB KINYOUN CARBOLFUCHSIN receive FDA 510(k) clearance?
TB KINYOUN CARBOLFUCHSIN received FDA 510(k) clearance on 1987-07-29, under 510(k) number K872187.
Who is the listed applicant for TB KINYOUN CARBOLFUCHSIN?
The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TB KINYOUN CARBOLFUCHSIN?
The FDA product code for TB KINYOUN CARBOLFUCHSIN is JTS.
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 Remel Co. 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: JTS)
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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