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FDA 510(k)

JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION

K-Number: K853327 · 1985-08-21

Decision Date1985-08-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION 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 1985-08-21 under 510(k) number K853327. 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 JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION?

JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION is a medical device that received FDA 510(k) clearance on 1985-08-21. The listed applicant is Jufrey Multimed Corp.. The 510(k) number is K853327.

When did JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION receive FDA 510(k) clearance?

JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION received FDA 510(k) clearance on 1985-08-21, under 510(k) number K853327.

Who is the listed applicant for JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION?

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 JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION?

The FDA product code for JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION 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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