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FDA 510(k)

MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE

K-Number: K000728 · 2000-03-21

ApplicantMedtronic Xomed
Decision Date2000-03-21
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Xomed. It received FDA 510(k) clearance on 2000-03-21 under 510(k) number K000728. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE?

MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE is a medical device that received FDA 510(k) clearance on 2000-03-21. The listed applicant is Medtronic Xomed. The 510(k) number is K000728.

When did MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE receive FDA 510(k) clearance?

MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE received FDA 510(k) clearance on 2000-03-21, under 510(k) number K000728.

Who is the listed applicant for MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE?

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

What is the FDA product code for MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE?

The FDA product code for MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE is FST.

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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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