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FDA 510(k)

SAFELINE MULTIDOSE VIAL ADAPTER

K-Number: K955595 · 1996-03-06

ApplicantMcgaw, Inc.
Decision Date1996-03-06
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFELINE MULTIDOSE VIAL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Mcgaw, Inc.. It received FDA 510(k) clearance on 1996-03-06 under 510(k) number K955595. 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 SAFELINE MULTIDOSE VIAL ADAPTER?

SAFELINE MULTIDOSE VIAL ADAPTER is a medical device that received FDA 510(k) clearance on 1996-03-06. The listed applicant is Mcgaw, Inc.. The 510(k) number is K955595.

When did SAFELINE MULTIDOSE VIAL ADAPTER receive FDA 510(k) clearance?

SAFELINE MULTIDOSE VIAL ADAPTER received FDA 510(k) clearance on 1996-03-06, under 510(k) number K955595.

Who is the listed applicant for SAFELINE MULTIDOSE VIAL ADAPTER?

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

What is the FDA product code for SAFELINE MULTIDOSE VIAL ADAPTER?

The FDA product code for SAFELINE MULTIDOSE VIAL ADAPTER is LHI.

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Other records listing Mcgaw, 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.

K972678MILLENNIUM CRT INFUSION PUMP AND MILLENNIUM CRT INFUSION PUMP ADMINISTRATION SETSK955594SAFELINE I.V. BAG ACCESS DEVICEK941244SAFELINE SYSTEM TURN LOCK CANNULAK932165INTRAVASCULAR ADMINISTRATION SETK931377SAFELINE SYSTEM IV ADMINISTRATION SETS & COMPONENTK932856IRRIGATION ACCESS CAP

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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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