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FDA 510(k)

SIGHTSURE OPERATIONAL INDICATOR, MODEL SS301

K-Number: K072550 · 2007-12-07

ApplicantMedevice, Inc.
Decision Date2007-12-07
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SIGHTSURE OPERATIONAL INDICATOR, MODEL SS301 is the device name listed in this FDA 510(k) record. The listed applicant is Medevice, Inc.. It received FDA 510(k) clearance on 2007-12-07 under 510(k) number K072550. 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 OPERATIONAL INDICATOR, MODEL SS301?

SIGHTSURE OPERATIONAL INDICATOR, MODEL SS301 is a medical device that received FDA 510(k) clearance on 2007-12-07. The listed applicant is Medevice, Inc.. The 510(k) number is K072550.

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

SIGHTSURE OPERATIONAL INDICATOR, MODEL SS301 received FDA 510(k) clearance on 2007-12-07, under 510(k) number K072550.

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

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

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

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

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Related Devices (Code: KNT)

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.

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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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