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FDA 510(k)

DOUBLE LUMEN TRANSFER DEVICE

K-Number: K830970 · 1983-04-12

ApplicantCodan Trading Co.
Decision Date1983-04-12
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DOUBLE LUMEN TRANSFER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Codan Trading Co.. It received FDA 510(k) clearance on 1983-04-12 under 510(k) number K830970. 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 DOUBLE LUMEN TRANSFER DEVICE?

DOUBLE LUMEN TRANSFER DEVICE is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Codan Trading Co.. The 510(k) number is K830970.

When did DOUBLE LUMEN TRANSFER DEVICE receive FDA 510(k) clearance?

DOUBLE LUMEN TRANSFER DEVICE received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830970.

Who is the listed applicant for DOUBLE LUMEN TRANSFER DEVICE?

The FDA 510(k) record lists Codan Trading Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOUBLE LUMEN TRANSFER DEVICE?

The FDA product code for DOUBLE LUMEN TRANSFER DEVICE 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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