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FDA 510(k)

ANGELTOUCH VENTED IV ADMINISTRATION SET

K-Number: K012189 · 2002-03-05

ApplicantAngiplast Private , Ltd.
Decision Date2002-03-05
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANGELTOUCH VENTED IV ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Angiplast Private , Ltd.. It received FDA 510(k) clearance on 2002-03-05 under 510(k) number K012189. 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 ANGELTOUCH VENTED IV ADMINISTRATION SET?

ANGELTOUCH VENTED IV ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 2002-03-05. The listed applicant is Angiplast Private , Ltd.. The 510(k) number is K012189.

When did ANGELTOUCH VENTED IV ADMINISTRATION SET receive FDA 510(k) clearance?

ANGELTOUCH VENTED IV ADMINISTRATION SET received FDA 510(k) clearance on 2002-03-05, under 510(k) number K012189.

Who is the listed applicant for ANGELTOUCH VENTED IV ADMINISTRATION SET?

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

What is the FDA product code for ANGELTOUCH VENTED IV ADMINISTRATION SET?

The FDA product code for ANGELTOUCH VENTED IV ADMINISTRATION SET is LHI.

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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

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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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