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FDA 510(k)

ECT CARBON FIBER PALLET, MODIFICATION

K-Number: K912481 · 1991-08-02

Decision Date1991-08-02
Product CodeIYZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECT CARBON FIBER PALLET, MODIFICATION 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 1991-08-02 under 510(k) number K912481. 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 CARBON FIBER PALLET, MODIFICATION?

ECT CARBON FIBER PALLET, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-08-02. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K912481.

When did ECT CARBON FIBER PALLET, MODIFICATION receive FDA 510(k) clearance?

ECT CARBON FIBER PALLET, MODIFICATION received FDA 510(k) clearance on 1991-08-02, under 510(k) number K912481.

Who is the listed applicant for ECT CARBON FIBER PALLET, MODIFICATION?

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 CARBON FIBER PALLET, MODIFICATION?

The FDA product code for ECT CARBON FIBER PALLET, MODIFICATION 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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