Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALPHA PLASMA TRANSFER SET

K-Number: K820447 · 1982-04-14

Decision Date1982-04-14
Product CodeKSB
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ALPHA PLASMA TRANSFER SET is the device name listed in this FDA 510(k) record. The listed applicant is Alpha Therapeutic Corp.. It received FDA 510(k) clearance on 1982-04-14 under 510(k) number K820447. The device is classified under product code KSB. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALPHA PLASMA TRANSFER SET?

ALPHA PLASMA TRANSFER SET is a medical device that received FDA 510(k) clearance on 1982-04-14. The listed applicant is Alpha Therapeutic Corp.. The 510(k) number is K820447.

When did ALPHA PLASMA TRANSFER SET receive FDA 510(k) clearance?

ALPHA PLASMA TRANSFER SET received FDA 510(k) clearance on 1982-04-14, under 510(k) number K820447.

Who is the listed applicant for ALPHA PLASMA TRANSFER 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 PLASMA TRANSFER SET?

The FDA product code for ALPHA PLASMA TRANSFER SET is KSB.

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.

View all 8 devices →

Related Devices (Code: KSB)

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.

↑