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FDA 510(k)

UROSKOP D1, UROSKOP D2, AND UROSKOP D3

K-Number: K923049 · 1992-09-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1992-09-15
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UROSKOP D1, UROSKOP D2, AND UROSKOP D3 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1992-09-15 under 510(k) number K923049. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROSKOP D1, UROSKOP D2, AND UROSKOP D3?

UROSKOP D1, UROSKOP D2, AND UROSKOP D3 is a medical device that received FDA 510(k) clearance on 1992-09-15. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K923049.

When did UROSKOP D1, UROSKOP D2, AND UROSKOP D3 receive FDA 510(k) clearance?

UROSKOP D1, UROSKOP D2, AND UROSKOP D3 received FDA 510(k) clearance on 1992-09-15, under 510(k) number K923049.

Who is the listed applicant for UROSKOP D1, UROSKOP D2, AND UROSKOP D3?

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

What is the FDA product code for UROSKOP D1, UROSKOP D2, AND UROSKOP D3?

The FDA product code for UROSKOP D1, UROSKOP D2, AND UROSKOP D3 is OWB.

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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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