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FDA 510(k)

VEINOPLUS NEUROMUSCULAR STIMULATOR

K-Number: K072252 · 2008-01-30

ApplicantAd Rem Technology Sarl
Decision Date2008-01-30
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VEINOPLUS NEUROMUSCULAR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ad Rem Technology Sarl. It received FDA 510(k) clearance on 2008-01-30 under 510(k) number K072252. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEINOPLUS NEUROMUSCULAR STIMULATOR?

VEINOPLUS NEUROMUSCULAR STIMULATOR is a medical device that received FDA 510(k) clearance on 2008-01-30. The listed applicant is Ad Rem Technology Sarl. The 510(k) number is K072252.

When did VEINOPLUS NEUROMUSCULAR STIMULATOR receive FDA 510(k) clearance?

VEINOPLUS NEUROMUSCULAR STIMULATOR received FDA 510(k) clearance on 2008-01-30, under 510(k) number K072252.

Who is the listed applicant for VEINOPLUS NEUROMUSCULAR STIMULATOR?

The FDA 510(k) record lists Ad Rem Technology Sarl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VEINOPLUS NEUROMUSCULAR STIMULATOR?

The FDA product code for VEINOPLUS NEUROMUSCULAR STIMULATOR is IPF.

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Related Devices (Code: IPF)

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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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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