FDA 510(k)

MED-TAB

K-Number: K173241 · 2018-03-23

Decision Date2018-03-23

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MED-TAB is the device name listed in this FDA 510(k) record. The listed applicant is Plum Medical Solutions GmbH. It received FDA 510(k) clearance on 2018-03-23 under 510(k) number K173241. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-TAB?

MED-TAB is a medical device that received FDA 510(k) clearance on 2018-03-23. The listed applicant is Plum Medical Solutions GmbH. The 510(k) number is K173241.

When did MED-TAB receive FDA 510(k) clearance?

MED-TAB received FDA 510(k) clearance on 2018-03-23, under 510(k) number K173241.

Who is the listed applicant for MED-TAB?

The FDA 510(k) record lists Plum Medical Solutions GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED-TAB?

The FDA product code for MED-TAB is LLZ.

Related Devices (Code: LLZ)

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.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

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.