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FDA 510(k)

MED CONTOUR

K-Number: K091615 · 2010-05-06

ApplicantGeneral Project S.R.L.
Decision Date2010-05-06
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MED CONTOUR is the device name listed in this FDA 510(k) record. The listed applicant is General Project S.R.L.. It received FDA 510(k) clearance on 2010-05-06 under 510(k) number K091615. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED CONTOUR?

MED CONTOUR is a medical device that received FDA 510(k) clearance on 2010-05-06. The listed applicant is General Project S.R.L.. The 510(k) number is K091615.

When did MED CONTOUR receive FDA 510(k) clearance?

MED CONTOUR received FDA 510(k) clearance on 2010-05-06, under 510(k) number K091615.

Who is the listed applicant for MED CONTOUR?

The FDA 510(k) record lists General Project S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED CONTOUR?

The FDA product code for MED CONTOUR is IMI.

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Other records listing General Project S.R.L. 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.

K161502MC1 PlusK062312AXIOM PULSED LIGHT SYSTEMK053041MED SCULPTK051508MED FLASH II INTENSE PULSED LIGHT SYSTEM.

Related Devices (Code: IMI)

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.

K240788Ultrasound StimulatorJkh Health Co., Ltd.K230472Sonopuls 190Enraf-Nonius, B.V.K222098ManaSport+Manamed, Inc.K210284ManaSportManamed, Inc.K202788Sonomed IV, Sonomed VCarci Industria E Comercio DE Aparelhos Cirurgicos E OrtoK160378BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)Brh Medical , Ltd.

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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