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FDA 510(k)

OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM

K-Number: K941919 · 1994-06-17

ApplicantOktas
Decision Date1994-06-17
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Oktas. It received FDA 510(k) clearance on 1994-06-17 under 510(k) number K941919. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM?

OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Oktas. The 510(k) number is K941919.

When did OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM receive FDA 510(k) clearance?

OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM received FDA 510(k) clearance on 1994-06-17, under 510(k) number K941919.

Who is the listed applicant for OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM?

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

What is the FDA product code for OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM?

The FDA product code for OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM is FET.

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 Oktas 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 7 devices →

Related Devices (Code: FET)

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

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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