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FDA 510(k)

UROSKOP A AND B

K-Number: K781532 · 1978-09-14

ApplicantSiemens Corp.
Decision Date1978-09-14
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UROSKOP A AND B is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781532. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROSKOP A AND B?

UROSKOP A AND B is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Siemens Corp.. The 510(k) number is K781532.

When did UROSKOP A AND B receive FDA 510(k) clearance?

UROSKOP A AND B received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781532.

Who is the listed applicant for UROSKOP A AND B?

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

What is the FDA product code for UROSKOP A AND B?

The FDA product code for UROSKOP A AND B is IXR.

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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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