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FDA 510(k)

FLOW-EZE BLUNT CANNULA (1999BC)

K-Number: K972538 · 1998-07-15

ApplicantAcacia, Inc.
Decision Date1998-07-15
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLOW-EZE BLUNT CANNULA (1999BC) is the device name listed in this FDA 510(k) record. The listed applicant is Acacia, Inc.. It received FDA 510(k) clearance on 1998-07-15 under 510(k) number K972538. 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 FLOW-EZE BLUNT CANNULA (1999BC)?

FLOW-EZE BLUNT CANNULA (1999BC) is a medical device that received FDA 510(k) clearance on 1998-07-15. The listed applicant is Acacia, Inc.. The 510(k) number is K972538.

When did FLOW-EZE BLUNT CANNULA (1999BC) receive FDA 510(k) clearance?

FLOW-EZE BLUNT CANNULA (1999BC) received FDA 510(k) clearance on 1998-07-15, under 510(k) number K972538.

Who is the listed applicant for FLOW-EZE BLUNT CANNULA (1999BC)?

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

What is the FDA product code for FLOW-EZE BLUNT CANNULA (1999BC)?

The FDA product code for FLOW-EZE BLUNT CANNULA (1999BC) is FMI.

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Other records listing Acacia, 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.

K122449ENTERAL NUTRITION WARMERK111381MEDI-SIS SYRINGE INFUSION SYSTEMK103165BLOOD SAMPLING SETK092986ACACIA PISTON SYRINGEK931095SPRING LOADED SYRINGEK912771ACACIAS PHARM/PUMP

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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

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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