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FDA 510(k)

PeriView FLEX

K-Number: K171232 · 2017-09-21

ApplicantOlympus Surgical Technologies America
Decision Date2017-09-21
Product CodeKTI
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PeriView FLEX is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Surgical Technologies America. It received FDA 510(k) clearance on 2017-09-21 under 510(k) number K171232. The device is classified under product code KTI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PeriView FLEX?

PeriView FLEX is a medical device that received FDA 510(k) clearance on 2017-09-21. The listed applicant is Olympus Surgical Technologies America. The 510(k) number is K171232.

When did PeriView FLEX receive FDA 510(k) clearance?

PeriView FLEX received FDA 510(k) clearance on 2017-09-21, under 510(k) number K171232.

Who is the listed applicant for PeriView FLEX?

The FDA 510(k) record lists Olympus Surgical Technologies America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PeriView FLEX?

The FDA product code for PeriView FLEX is KTI.

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Related Devices (Code: KTI)

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

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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