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FDA 510(k)

REHASTIM & REHAMOVE

K-Number: K073237 · 2007-12-27

ApplicantHasomed GmbH
Decision Date2007-12-27
Product CodeGZI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

REHASTIM & REHAMOVE is the device name listed in this FDA 510(k) record. The listed applicant is Hasomed GmbH. It received FDA 510(k) clearance on 2007-12-27 under 510(k) number K073237. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REHASTIM & REHAMOVE?

REHASTIM & REHAMOVE is a medical device that received FDA 510(k) clearance on 2007-12-27. The listed applicant is Hasomed GmbH. The 510(k) number is K073237.

When did REHASTIM & REHAMOVE receive FDA 510(k) clearance?

REHASTIM & REHAMOVE received FDA 510(k) clearance on 2007-12-27, under 510(k) number K073237.

Who is the listed applicant for REHASTIM & REHAMOVE?

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

What is the FDA product code for REHASTIM & REHAMOVE?

The FDA product code for REHASTIM & REHAMOVE is GZI.

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.

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Other records listing Hasomed GmbH 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.

K162683RehaStim 2K112844REHASTIM 2, REHAMOVE 2

Related Devices (Code: GZI)

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.

K242704Synchrony (20-3000)Synapse Biomedical, Inc.K243828CIONIC NEURAL SLEEVE (NS-200)Cionic, Inc.K240632Neuvotion NeuStim NN-01Neuvotion, Inc.K233006MyndMove, MyndMove 2.0Myndtec, Inc.K230997EvoWalk 1.0 SystemEvolution Devices, Inc.K221823Cionic Neural Sleeve NS-100Cionic

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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