BENT WINGED MINI-VOL INFUSION SET
K-Number: K842143 · 1984-07-20
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Device Summary
Frequently Asked Questions
What is the BENT WINGED MINI-VOL INFUSION SET?
BENT WINGED MINI-VOL INFUSION SET is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is Med Fusion Systems, Inc.. The 510(k) number is K842143.
When did BENT WINGED MINI-VOL INFUSION SET receive FDA 510(k) clearance?
BENT WINGED MINI-VOL INFUSION SET received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842143.
Who is the listed applicant for BENT WINGED MINI-VOL INFUSION SET?
The FDA 510(k) record lists Med Fusion Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BENT WINGED MINI-VOL INFUSION SET?
The FDA product code for BENT WINGED MINI-VOL INFUSION 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 Med Fusion Systems, 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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