GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC
K-Number: K832257 · 1983-10-28
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Device Summary
Frequently Asked Questions
What is the GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC?
GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Gelco Diagnostics, Inc.. The 510(k) number is K832257.
When did GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC receive FDA 510(k) clearance?
GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC received FDA 510(k) clearance on 1983-10-28, under 510(k) number K832257.
Who is the listed applicant for GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC?
The FDA 510(k) record lists Gelco Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC?
The FDA product code for GOAT ANTI-HUMAN IGA A CHAIN SPECIFIC is CZN.
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 Gelco Diagnostics, 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: CZN)
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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