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FDA 510(k)

PHASEAL

K-Number: K023747 · 2002-11-15

ApplicantCarmel Pharma Ab.
Decision Date2002-11-15
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHASEAL is the device name listed in this FDA 510(k) record. The listed applicant is Carmel Pharma Ab.. It received FDA 510(k) clearance on 2002-11-15 under 510(k) number K023747. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHASEAL?

PHASEAL is a medical device that received FDA 510(k) clearance on 2002-11-15. The listed applicant is Carmel Pharma Ab.. The 510(k) number is K023747.

When did PHASEAL receive FDA 510(k) clearance?

PHASEAL received FDA 510(k) clearance on 2002-11-15, under 510(k) number K023747.

Who is the listed applicant for PHASEAL?

The FDA 510(k) record lists Carmel Pharma Ab. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHASEAL?

The FDA product code for PHASEAL is LHI.

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Other records listing Carmel Pharma Ab. 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.

K110023INFUSION ADAPTER C100K092782INJECTOR LUER, MODEL N34, INJECTOR LUER LOCK, MODEL N35, INJECTOR LUER LOCK, N35C, CONNECTOR LUER LOCK, MODEL C35,K090634PHASEAL PROTECTOR P14, P21, P28 AND P50K060866PHASEAL - CLOSED SYSTEM FOR THE PREPARATION AND ADMINISTRATION OF PARENTERAL DRUGSK001368PROTECTOR 21, PROTECTOR 50, PROTECTOR 14, INJECTOR LUER LOCK, INFUSION ADAPTERK980381PHASEAL, CLOSED SYSTEM FORHANDLING OF PARENTERAL DRUGS, ADDITIONAL ADMINISTRATION DEVICES. C80 INFUSION ADAPTER, A10 PRO

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Related Devices (Code: LHI)

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.

K252987ADRx™ Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LPK251715FlowArt® Vial Access Device VentedAsset MedikalK251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLCK243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

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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