ECT PROCESSOR
K-Number: K832737 · 1983-09-29
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Device Summary
Frequently Asked Questions
What is the ECT PROCESSOR?
ECT PROCESSOR is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K832737.
When did ECT PROCESSOR receive FDA 510(k) clearance?
ECT PROCESSOR received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832737.
Who is the listed applicant for ECT PROCESSOR?
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 PROCESSOR?
The FDA product code for ECT PROCESSOR is JWM.
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: JWM)
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.
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