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FDA 510(k)

MP VIAL ADAPTER 13MM

K-Number: K130179 · 2013-08-08

Decision Date2013-08-08
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MP VIAL ADAPTER 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 2013-08-08 under 510(k) number K130179. 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 MP VIAL ADAPTER 13MM?

MP VIAL ADAPTER 13MM is a medical device that received FDA 510(k) clearance on 2013-08-08. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K130179.

When did MP VIAL ADAPTER 13MM receive FDA 510(k) clearance?

MP VIAL ADAPTER 13MM received FDA 510(k) clearance on 2013-08-08, under 510(k) number K130179.

Who is the listed applicant for MP VIAL ADAPTER 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 MP VIAL ADAPTER 13MM?

The FDA product code for MP VIAL ADAPTER 13MM 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 Medimop Medical Projects, Ltd. 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 11 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

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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