THERAPY BENCH
K-Number: K812319 · 1981-08-31
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Device Summary
Frequently Asked Questions
What is the THERAPY BENCH?
THERAPY BENCH is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Kaye Products, Inc.. The 510(k) number is K812319.
When did THERAPY BENCH receive FDA 510(k) clearance?
THERAPY BENCH received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812319.
Who is the listed applicant for THERAPY BENCH?
The FDA 510(k) record lists Kaye Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERAPY BENCH?
The FDA product code for THERAPY BENCH is IOD.
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 Kaye Products, 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: IOD)
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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