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FDA 510(k)

Vented Vial Adapter Transfer Device - 13mm

K-Number: K160503 · 2016-05-04

Decision Date2016-05-04
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vented Vial Adapter Transfer Device - 13mm is the device name listed in this FDA 510(k) record. The listed applicant is Medimop Medical Projects, Ltd.. It received FDA 510(k) clearance on 2016-05-04 under 510(k) number K160503. 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 Vented Vial Adapter Transfer Device - 13mm?

Vented Vial Adapter Transfer Device - 13mm is a medical device that received FDA 510(k) clearance on 2016-05-04. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K160503.

When did Vented Vial Adapter Transfer Device - 13mm receive FDA 510(k) clearance?

Vented Vial Adapter Transfer Device - 13mm received FDA 510(k) clearance on 2016-05-04, under 510(k) number K160503.

Who is the listed applicant for Vented Vial Adapter Transfer Device - 13mm?

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

What is the FDA product code for Vented Vial Adapter Transfer Device - 13mm?

The FDA product code for Vented Vial Adapter Transfer Device - 13mm is LHI.

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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