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FDA 510(k)

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F)

K-Number: K861518 · 1986-05-27

Decision Date1986-05-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F) is the device name listed in this FDA 510(k) record. The listed applicant is Jufrey Multimed Corp.. It received FDA 510(k) clearance on 1986-05-27 under 510(k) number K861518. 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 UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F)?

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F) is a medical device that received FDA 510(k) clearance on 1986-05-27. The listed applicant is Jufrey Multimed Corp.. The 510(k) number is K861518.

When did UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F) receive FDA 510(k) clearance?

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F) received FDA 510(k) clearance on 1986-05-27, under 510(k) number K861518.

Who is the listed applicant for UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F)?

The FDA 510(k) record lists Jufrey Multimed Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F)?

The FDA product code for UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F) 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 Jufrey Multimed Corp. 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 7 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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