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FDA 510(k)

LITEPORT LP100 SURGICAL ILLUMINATOR

K-Number: K041621 · 2004-09-13

ApplicantMedical Vision Industries, Inc.
Decision Date2004-09-13
Product CodeFTF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LITEPORT LP100 SURGICAL ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Vision Industries, Inc.. It received FDA 510(k) clearance on 2004-09-13 under 510(k) number K041621. The device is classified under product code FTF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITEPORT LP100 SURGICAL ILLUMINATOR?

LITEPORT LP100 SURGICAL ILLUMINATOR is a medical device that received FDA 510(k) clearance on 2004-09-13. The listed applicant is Medical Vision Industries, Inc.. The 510(k) number is K041621.

When did LITEPORT LP100 SURGICAL ILLUMINATOR receive FDA 510(k) clearance?

LITEPORT LP100 SURGICAL ILLUMINATOR received FDA 510(k) clearance on 2004-09-13, under 510(k) number K041621.

Who is the listed applicant for LITEPORT LP100 SURGICAL ILLUMINATOR?

The FDA 510(k) record lists Medical Vision Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITEPORT LP100 SURGICAL ILLUMINATOR?

The FDA product code for LITEPORT LP100 SURGICAL ILLUMINATOR is FTF.

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Related Devices (Code: FTF)

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.

K840371FLEXIBLE ILLUMINATOR 5Suncoast Medical Manufacturers, Inc.K840372FLEXIBLE ILLUMINATOR 15Suncoast Medical Manufacturers, Inc.K840373FLEXIBLE ILLUMINATOR 10Suncoast Medical Manufacturers, Inc.

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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