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FDA 510(k)

ORBITER II CCI/SPECT ORBITER II CCI/SPECT

K-Number: K010137 · 2001-02-13

Decision Date2001-02-13
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ORBITER II CCI/SPECT ORBITER II CCI/SPECT 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 2001-02-13 under 510(k) number K010137. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORBITER II CCI/SPECT ORBITER II CCI/SPECT?

ORBITER II CCI/SPECT ORBITER II CCI/SPECT is a medical device that received FDA 510(k) clearance on 2001-02-13. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K010137.

When did ORBITER II CCI/SPECT ORBITER II CCI/SPECT receive FDA 510(k) clearance?

ORBITER II CCI/SPECT ORBITER II CCI/SPECT received FDA 510(k) clearance on 2001-02-13, under 510(k) number K010137.

Who is the listed applicant for ORBITER II CCI/SPECT ORBITER II CCI/SPECT?

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 ORBITER II CCI/SPECT ORBITER II CCI/SPECT?

The FDA product code for ORBITER II CCI/SPECT ORBITER II CCI/SPECT is KPS.

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.

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Related Devices (Code: KPS)

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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