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FDA 510(k)

BOSTON BLOOD DONOR SETS

K-Number: K822410 · 1982-09-30

Decision Date1982-09-30
Product CodeBRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOSTON BLOOD DONOR SETS is the device name listed in this FDA 510(k) record. The listed applicant is The Boston Medical Group. It received FDA 510(k) clearance on 1982-09-30 under 510(k) number K822410. The device is classified under product code BRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOSTON BLOOD DONOR SETS?

BOSTON BLOOD DONOR SETS is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is The Boston Medical Group. The 510(k) number is K822410.

When did BOSTON BLOOD DONOR SETS receive FDA 510(k) clearance?

BOSTON BLOOD DONOR SETS received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822410.

Who is the listed applicant for BOSTON BLOOD DONOR SETS?

The FDA 510(k) record lists The Boston Medical Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOSTON BLOOD DONOR SETS?

The FDA product code for BOSTON BLOOD DONOR SETS 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 The Boston Medical Group 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

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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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