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FDA 510(k)

SIREMOBIL ISO-C 3D

K-Number: K032280 · 2003-09-10

ApplicantSiemens AG
Decision Date2003-09-10
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIREMOBIL ISO-C 3D is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG. It received FDA 510(k) clearance on 2003-09-10 under 510(k) number K032280. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIREMOBIL ISO-C 3D?

SIREMOBIL ISO-C 3D is a medical device that received FDA 510(k) clearance on 2003-09-10. The listed applicant is Siemens AG. The 510(k) number is K032280.

When did SIREMOBIL ISO-C 3D receive FDA 510(k) clearance?

SIREMOBIL ISO-C 3D received FDA 510(k) clearance on 2003-09-10, under 510(k) number K032280.

Who is the listed applicant for SIREMOBIL ISO-C 3D?

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

What is the FDA product code for SIREMOBIL ISO-C 3D?

The FDA product code for SIREMOBIL ISO-C 3D is IZL.

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Other records listing Siemens AG as applicant

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K123375SYNGO.VIAK110366SYNGO.CT CARDIAC FUNCTIONK071310SYNGO CT ONCOLOGY SOFTWARE PACKAGEK063507SYNGO NEURO PBV CTK063373FLEX LOOP COIL SET 3TK053024SYNGO NEURO DSA CT

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Related Devices (Code: IZL)

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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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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