CORRECT FLO INTRAVASCULAR ADMINISTRATION SET
K-Number: K850506 · 1985-04-01
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Device Summary
Frequently Asked Questions
What is the CORRECT FLO INTRAVASCULAR ADMINISTRATION SET?
CORRECT FLO INTRAVASCULAR ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Biomedical Dynamics, Inc.. The 510(k) number is K850506.
When did CORRECT FLO INTRAVASCULAR ADMINISTRATION SET receive FDA 510(k) clearance?
CORRECT FLO INTRAVASCULAR ADMINISTRATION SET received FDA 510(k) clearance on 1985-04-01, under 510(k) number K850506.
Who is the listed applicant for CORRECT FLO INTRAVASCULAR ADMINISTRATION SET?
The FDA 510(k) record lists Biomedical Dynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORRECT FLO INTRAVASCULAR ADMINISTRATION SET?
The FDA product code for CORRECT FLO INTRAVASCULAR ADMINISTRATION SET 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 Biomedical Dynamics, 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: 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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