Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BENT WINGED MINI-VOL INFUSION SET

K-Number: K842143 · 1984-07-20

Decision Date1984-07-20
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BENT WINGED MINI-VOL INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Med Fusion Systems, Inc.. It received FDA 510(k) clearance on 1984-07-20 under 510(k) number K842143. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 22 devices →

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.

↑