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FDA 510(k)

SIEMEMNS INFINITY ETC02 POD

K-Number: K992116 · 2000-01-12

Decision Date2000-01-12
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMEMNS INFINITY ETC02 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 2000-01-12 under 510(k) number K992116. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMEMNS INFINITY ETC02 POD?

SIEMEMNS INFINITY ETC02 POD is a medical device that received FDA 510(k) clearance on 2000-01-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K992116.

When did SIEMEMNS INFINITY ETC02 POD receive FDA 510(k) clearance?

SIEMEMNS INFINITY ETC02 POD received FDA 510(k) clearance on 2000-01-12, under 510(k) number K992116.

Who is the listed applicant for SIEMEMNS INFINITY ETC02 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 SIEMEMNS INFINITY ETC02 POD?

The FDA product code for SIEMEMNS INFINITY ETC02 POD is CCK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Siemens Medical Solutions USA, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 732 devices →

Related Devices (Code: CCK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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