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FDA 510(k)

SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE

K-Number: K032598 · 2003-11-24

ApplicantSynergetics, Inc.
Decision Date2003-11-24
Product CodeMPA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Synergetics, Inc.. It received FDA 510(k) clearance on 2003-11-24 under 510(k) number K032598. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE?

SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE is a medical device that received FDA 510(k) clearance on 2003-11-24. The listed applicant is Synergetics, Inc.. The 510(k) number is K032598.

When did SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE receive FDA 510(k) clearance?

SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE received FDA 510(k) clearance on 2003-11-24, under 510(k) number K032598.

Who is the listed applicant for SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE?

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

What is the FDA product code for SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE?

The FDA product code for SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE is MPA.

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Related Devices (Code: MPA)

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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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