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FDA 510(k)

20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500

K-Number: K100640 · 2010-07-22

Decision Date2010-07-22
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500 is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2010-07-22 under 510(k) number K100640. 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 20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500?

20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500 is a medical device that received FDA 510(k) clearance on 2010-07-22. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K100640.

When did 20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500 receive FDA 510(k) clearance?

20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500 received FDA 510(k) clearance on 2010-07-22, under 510(k) number K100640.

Who is the listed applicant for 20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500?

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

What is the FDA product code for 20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500?

The FDA product code for 20 MMVIAL FLUID TRANSFER ADAPTER, MODEL 7E2500 is LHI.

Related Clinical Trials

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.

Other records listing B.Braun Medical, 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.

View all 142 devices →

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.

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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