BOSTON SOLUTION INFUSION SETS
K-Number: K822406 · 1982-09-30
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Device Summary
Frequently Asked Questions
What is the BOSTON SOLUTION INFUSION SETS?
BOSTON SOLUTION INFUSION 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 K822406.
When did BOSTON SOLUTION INFUSION SETS receive FDA 510(k) clearance?
BOSTON SOLUTION INFUSION SETS received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822406.
Who is the listed applicant for BOSTON SOLUTION INFUSION 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 SOLUTION INFUSION SETS?
The FDA product code for BOSTON SOLUTION INFUSION SETS is FPA.
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: FPA)
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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