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FDA 510(k)

SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER

K-Number: K012461 · 2001-08-17

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2001-08-17
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER 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 2001-08-17 under 510(k) number K012461. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER?

SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER is a medical device that received FDA 510(k) clearance on 2001-08-17. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K012461.

When did SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER receive FDA 510(k) clearance?

SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER received FDA 510(k) clearance on 2001-08-17, under 510(k) number K012461.

Who is the listed applicant for SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER?

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 SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER?

The FDA product code for SIEMENS INFINITY MIB II DUO PROTOCOL CONVERTER is DSI.

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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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