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FDA 510(k)

SIEMENS ANGIOTRON

K-Number: K811587 · 1981-07-10

ApplicantSiemens Corp.
Decision Date1981-07-10
Product CodeIXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS ANGIOTRON is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-07-10 under 510(k) number K811587. The device is classified under product code IXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS ANGIOTRON?

SIEMENS ANGIOTRON is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Siemens Corp.. The 510(k) number is K811587.

When did SIEMENS ANGIOTRON receive FDA 510(k) clearance?

SIEMENS ANGIOTRON received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811587.

Who is the listed applicant for SIEMENS ANGIOTRON?

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 SIEMENS ANGIOTRON?

The FDA product code for SIEMENS ANGIOTRON is IXO.

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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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