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FDA 510(k)

CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT)

K-Number: K792637 · 1980-01-11

Decision Date1980-01-11
Product CodeKTS
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT) is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792637. The device is classified under product code KTS. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 69 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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