EXER-STIM CONTROLLER
K-Number: K822056 · 1982-10-06
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Device Summary
Frequently Asked Questions
What is the EXER-STIM CONTROLLER?
EXER-STIM CONTROLLER is a medical device that received FDA 510(k) clearance on 1982-10-06. The listed applicant is Th Charters, Inc.. The 510(k) number is K822056.
When did EXER-STIM CONTROLLER receive FDA 510(k) clearance?
EXER-STIM CONTROLLER received FDA 510(k) clearance on 1982-10-06, under 510(k) number K822056.
Who is the listed applicant for EXER-STIM CONTROLLER?
The FDA 510(k) record lists Th Charters, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXER-STIM CONTROLLER?
The FDA product code for EXER-STIM CONTROLLER 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 Th Charters, 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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