Decision Date2004-01-30
Product CodeFGB
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
OLYMPUS VIDEO URETEROSCOPE, NTSC is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Winter & Ibe GmbH. It received FDA 510(k) clearance on 2004-01-30 under 510(k) number K033651. The device is classified under product code FGB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the OLYMPUS VIDEO URETEROSCOPE, NTSC?
OLYMPUS VIDEO URETEROSCOPE, NTSC is a medical device that received FDA 510(k) clearance on 2004-01-30. The listed applicant is Olympus Winter & Ibe GmbH. The 510(k) number is K033651.
When did OLYMPUS VIDEO URETEROSCOPE, NTSC receive FDA 510(k) clearance?
OLYMPUS VIDEO URETEROSCOPE, NTSC received FDA 510(k) clearance on 2004-01-30, under 510(k) number K033651.
Who is the listed applicant for OLYMPUS VIDEO URETEROSCOPE, NTSC?
The FDA 510(k) record lists Olympus Winter & Ibe GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OLYMPUS VIDEO URETEROSCOPE, NTSC?
The FDA product code for OLYMPUS VIDEO URETEROSCOPE, NTSC is FGB.
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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.