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FDA 510(k)

SIEMENS INFINITY EEG POD

K-Number: K991012 · 1999-06-24

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1999-06-24
Product CodeOLT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SIEMENS INFINITY EEG POD 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 1999-06-24 under 510(k) number K991012. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS INFINITY EEG POD?

SIEMENS INFINITY EEG POD is a medical device that received FDA 510(k) clearance on 1999-06-24. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K991012.

When did SIEMENS INFINITY EEG POD receive FDA 510(k) clearance?

SIEMENS INFINITY EEG POD received FDA 510(k) clearance on 1999-06-24, under 510(k) number K991012.

Who is the listed applicant for SIEMENS INFINITY EEG POD?

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 EEG POD?

The FDA product code for SIEMENS INFINITY EEG POD is OLT.

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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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