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FDA 510(k)

OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES

K-Number: K862402 · 1987-02-03

Decision Date1987-02-03
Product CodeNVE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Medivators, Inc.. It received FDA 510(k) clearance on 1987-02-03 under 510(k) number K862402. The device is classified under product code NVE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES?

OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES is a medical device that received FDA 510(k) clearance on 1987-02-03. The listed applicant is Medivators, Inc.. The 510(k) number is K862402.

When did OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES receive FDA 510(k) clearance?

OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES received FDA 510(k) clearance on 1987-02-03, under 510(k) number K862402.

Who is the listed applicant for OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES?

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

What is the FDA product code for OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES?

The FDA product code for OTT DISINFECTOR FOR FLEXIBLE ENDOSCOPES is NVE.

Related Clinical Trials

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.

Other records listing Medivators, Inc. as applicant

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.

View all 9 devices →

Related Devices (Code: NVE)

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.

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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