PRESELECTED FLOW RATE I.V. SET
K-Number: K863304 · 1986-12-09
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Device Summary
Frequently Asked Questions
What is the PRESELECTED FLOW RATE I.V. SET?
PRESELECTED FLOW RATE I.V. SET is a medical device that received FDA 510(k) clearance on 1986-12-09. The listed applicant is Migada, Ltd.. The 510(k) number is K863304.
When did PRESELECTED FLOW RATE I.V. SET receive FDA 510(k) clearance?
PRESELECTED FLOW RATE I.V. SET received FDA 510(k) clearance on 1986-12-09, under 510(k) number K863304.
Who is the listed applicant for PRESELECTED FLOW RATE I.V. SET?
The FDA 510(k) record lists Migada, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRESELECTED FLOW RATE I.V. SET?
The FDA product code for PRESELECTED FLOW RATE I.V. 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 Migada, Ltd. 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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