TTI REHABILATATION GYM SYS
K-Number: K841112 · 1984-04-04
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Device Summary
Frequently Asked Questions
What is the TTI REHABILATATION GYM SYS?
TTI REHABILATATION GYM SYS is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Therapeutic Technologies, Inc.. The 510(k) number is K841112.
When did TTI REHABILATATION GYM SYS receive FDA 510(k) clearance?
TTI REHABILATATION GYM SYS received FDA 510(k) clearance on 1984-04-04, under 510(k) number K841112.
Who is the listed applicant for TTI REHABILATATION GYM SYS?
The FDA 510(k) record lists Therapeutic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TTI REHABILATATION GYM SYS?
The FDA product code for TTI REHABILATATION GYM SYS is IPF.
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 Therapeutic Technologies, 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: IPF)
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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