CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT)
K-Number: K792637 · 1980-01-11
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Device Summary
Frequently Asked Questions
What is the CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT)?
CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT) is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Union Carbide Corp.. The 510(k) number is K792637.
When did CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT) receive FDA 510(k) clearance?
CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT) received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792637.
Who is the listed applicant for CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT)?
The FDA 510(k) record lists Union Carbide Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT)?
The FDA product code for CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT) is KTS.
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 Union Carbide Corp. 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: KTS)
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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