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FDA 510(k)

SIGHTSURE OPERATION INDICATOR, MODEL SS301

K-Number: K993358 · 2000-03-15

ApplicantMedevices, Inc.
Decision Date2000-03-15
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SIGHTSURE OPERATION INDICATOR, MODEL SS301 is the device name listed in this FDA 510(k) record. The listed applicant is Medevices, Inc.. It received FDA 510(k) clearance on 2000-03-15 under 510(k) number K993358. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGHTSURE OPERATION INDICATOR, MODEL SS301?

SIGHTSURE OPERATION INDICATOR, MODEL SS301 is a medical device that received FDA 510(k) clearance on 2000-03-15. The listed applicant is Medevices, Inc.. The 510(k) number is K993358.

When did SIGHTSURE OPERATION INDICATOR, MODEL SS301 receive FDA 510(k) clearance?

SIGHTSURE OPERATION INDICATOR, MODEL SS301 received FDA 510(k) clearance on 2000-03-15, under 510(k) number K993358.

Who is the listed applicant for SIGHTSURE OPERATION INDICATOR, MODEL SS301?

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

What is the FDA product code for SIGHTSURE OPERATION INDICATOR, MODEL SS301?

The FDA product code for SIGHTSURE OPERATION INDICATOR, MODEL SS301 is KNT.

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Related Devices (Code: KNT)

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Official Source

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