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FDA 510(k)

TRANSFER DEVICE

K-Number: K853188 · 1985-08-21

ApplicantAdvance Medical Designs, Inc.
Decision Date1985-08-21
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRANSFER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Advance Medical Designs, Inc.. It received FDA 510(k) clearance on 1985-08-21 under 510(k) number K853188. 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 TRANSFER DEVICE?

TRANSFER DEVICE is a medical device that received FDA 510(k) clearance on 1985-08-21. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K853188.

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

TRANSFER DEVICE received FDA 510(k) clearance on 1985-08-21, under 510(k) number K853188.

Who is the listed applicant for TRANSFER DEVICE?

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

What is the FDA product code for TRANSFER DEVICE?

The FDA product code for TRANSFER DEVICE is LHI.

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Other records listing Advance Medical Designs, 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.

K223689Disposable Needle Guides and GridsK163050Advance Medical Designs, Inc. Sterile Ultrasound GelK053495EQUIPMENT SLUSH DRAPEK011265ULTRASOUND TRANSDUCER COVERK012168ADVANCE MEDICAL DESIGNS FLUID POUCHK011422SURGICAL DRAPES

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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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