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FDA 510(k)

ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL

K-Number: K903767 · 1990-09-07

Decision Date1990-09-07
Product CodeIYZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Gammasonics, Inc.. It received FDA 510(k) clearance on 1990-09-07 under 510(k) number K903767. The device is classified under product code IYZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL?

ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL is a medical device that received FDA 510(k) clearance on 1990-09-07. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K903767.

When did ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL receive FDA 510(k) clearance?

ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL received FDA 510(k) clearance on 1990-09-07, under 510(k) number K903767.

Who is the listed applicant for ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL?

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

What is the FDA product code for ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL?

The FDA product code for ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL is IYZ.

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 Gammasonics, 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 53 devices →

Related Devices (Code: IYZ)

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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