ECT CARBON FIBER PALLET, MODIFICATION
K-Number: K912481 · 1991-08-02
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement