TCT-1 TREATMENT COUCH
K-Number: K834201 · 1984-03-05
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Device Summary
Frequently Asked Questions
What is the TCT-1 TREATMENT COUCH?
TCT-1 TREATMENT COUCH is a medical device that received FDA 510(k) clearance on 1984-03-05. The listed applicant is Therados, Inc.. The 510(k) number is K834201.
When did TCT-1 TREATMENT COUCH receive FDA 510(k) clearance?
TCT-1 TREATMENT COUCH received FDA 510(k) clearance on 1984-03-05, under 510(k) number K834201.
Who is the listed applicant for TCT-1 TREATMENT COUCH?
The FDA 510(k) record lists Therados, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TCT-1 TREATMENT COUCH?
The FDA product code for TCT-1 TREATMENT COUCH is JAI.
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 Therados, 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: JAI)
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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