ALLIED ASSOCIATES THERAPEUTIC EXERSIE
K-Number: K842432 · 1984-08-01
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Device Summary
Frequently Asked Questions
What is the ALLIED ASSOCIATES THERAPEUTIC EXERSIE?
ALLIED ASSOCIATES THERAPEUTIC EXERSIE is a medical device that received FDA 510(k) clearance on 1984-08-01. The listed applicant is Allied Associates, Inc.. The 510(k) number is K842432.
When did ALLIED ASSOCIATES THERAPEUTIC EXERSIE receive FDA 510(k) clearance?
ALLIED ASSOCIATES THERAPEUTIC EXERSIE received FDA 510(k) clearance on 1984-08-01, under 510(k) number K842432.
Who is the listed applicant for ALLIED ASSOCIATES THERAPEUTIC EXERSIE?
The FDA 510(k) record lists Allied Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALLIED ASSOCIATES THERAPEUTIC EXERSIE?
The FDA product code for ALLIED ASSOCIATES THERAPEUTIC EXERSIE is BXB.
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 Allied Associates, 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: BXB)
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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