FDA 510(k)

SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT

K-Number: K912070 · 1992-04-23

Decision Date1992-04-23

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Electronics. It received FDA 510(k) clearance on 1992-04-23 under 510(k) number K912070. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT?

SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT is a medical device that received FDA 510(k) clearance on 1992-04-23. The listed applicant is Siemens Medical Electronics. The 510(k) number is K912070.

When did SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT receive FDA 510(k) clearance?

SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT received FDA 510(k) clearance on 1992-04-23, under 510(k) number K912070.

Who is the listed applicant for SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT?

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

What is the FDA product code for SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT?

The FDA product code for SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.