ALPHA Y-RECIPIENT SET
K-Number: K833294 · 1983-12-27
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Device Summary
Frequently Asked Questions
What is the ALPHA Y-RECIPIENT SET?
ALPHA Y-RECIPIENT SET is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Alpha Therapeutic Corp.. The 510(k) number is K833294.
When did ALPHA Y-RECIPIENT SET receive FDA 510(k) clearance?
ALPHA Y-RECIPIENT SET received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833294.
Who is the listed applicant for ALPHA Y-RECIPIENT SET?
The FDA 510(k) record lists Alpha Therapeutic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALPHA Y-RECIPIENT SET?
The FDA product code for ALPHA Y-RECIPIENT SET is BRZ.
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 Alpha Therapeutic 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: BRZ)
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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