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FDA 510(k)

SHROUDED PLASTIC CANNULA

K-Number: K952834 · 1995-10-03

ApplicantMedical Associates Network, Inc.
Decision Date1995-10-03
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHROUDED PLASTIC CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Medical Associates Network, Inc.. It received FDA 510(k) clearance on 1995-10-03 under 510(k) number K952834. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHROUDED PLASTIC CANNULA?

SHROUDED PLASTIC CANNULA is a medical device that received FDA 510(k) clearance on 1995-10-03. The listed applicant is Medical Associates Network, Inc.. The 510(k) number is K952834.

When did SHROUDED PLASTIC CANNULA receive FDA 510(k) clearance?

SHROUDED PLASTIC CANNULA received FDA 510(k) clearance on 1995-10-03, under 510(k) number K952834.

Who is the listed applicant for SHROUDED PLASTIC CANNULA?

The FDA 510(k) record lists Medical Associates Network, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHROUDED PLASTIC CANNULA?

The FDA product code for SHROUDED PLASTIC CANNULA is FMI.

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.

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Other records listing Medical Associates Network, 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.

K955821I.V. ADMINISTRATION SETSK953343NEEDLELESS INJECTION SITE

Related Devices (Code: FMI)

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.

K261266MOWANA™ Auto DuoPENTAMASTER MEDIQ SDN BHDK261719Promisemed X-Safety Pen NeedlePromisemed Hangzhou Meditech Co., Ltd.K262427Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety Type IIIB, Safety Type IV, Safety Type V, Ordinary Type VIA, Ordinary Type VIB, Ordinary Type VIC, Safety Type VII, Ordinary Type IB, Safety type VIII, Safety Type IX, Safety Type X, Ordinary Type XI, Safety Type XII)Hh Global Technology, Inc.K260933Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R, NR-S2016R, NR-S2025R, NR-S2038R, NR-S2051R, NR-S2116R, NR-S2125R, NR-S2138R, NR-S2151R, NR-S2216R, NR-S2225R, NR-S2238R, NR-S2251R, NR-S2316R, NR-S2325R, NR-S2338R, NR-S2351R, NR-S2516R, NR-S2525R, NR-S2538R, NR-S2551R, NR-S2516T, NR-S2525T, NR-S2538T, NR-S2551T)Hangzhou Qiantang Longyue Biotechnology Co., Ltd.K261829Profoject™ Dual-Safety Pen NeedlesCMT Health PTE., Ltd.K260739Profoject™ Pen Needles (Model A; Model B)CMT Health PTE., Ltd.

Official Source

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