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FDA 510(k)

THE FUGO BLADE FOR GLAUCOMA

K-Number: K041019 · 2004-10-08

ApplicantMedisurg , Ltd.
Decision Date2004-10-08
Product CodeNCR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE FUGO BLADE FOR GLAUCOMA is the device name listed in this FDA 510(k) record. The listed applicant is Medisurg , Ltd.. It received FDA 510(k) clearance on 2004-10-08 under 510(k) number K041019. The device is classified under product code NCR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE FUGO BLADE FOR GLAUCOMA?

THE FUGO BLADE FOR GLAUCOMA is a medical device that received FDA 510(k) clearance on 2004-10-08. The listed applicant is Medisurg , Ltd.. The 510(k) number is K041019.

When did THE FUGO BLADE FOR GLAUCOMA receive FDA 510(k) clearance?

THE FUGO BLADE FOR GLAUCOMA received FDA 510(k) clearance on 2004-10-08, under 510(k) number K041019.

Who is the listed applicant for THE FUGO BLADE FOR GLAUCOMA?

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

What is the FDA product code for THE FUGO BLADE FOR GLAUCOMA?

The FDA product code for THE FUGO BLADE FOR GLAUCOMA is NCR.

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Other records listing Medisurg , 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.

K063468THE FUGO BLADE FOR DENTISTRYK050933FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300K001498THE FUGO BLADE

Related Devices (Code: NCR)

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.

K050933FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300Medisurg , Ltd.K001498THE FUGO BLADEMedisurg , 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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