MODEL 1080 ROLLER MASSAGE TABLE
K-Number: K883357 · 1988-08-23
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Device Summary
Frequently Asked Questions
What is the MODEL 1080 ROLLER MASSAGE TABLE?
MODEL 1080 ROLLER MASSAGE TABLE is a medical device that received FDA 510(k) clearance on 1988-08-23. The listed applicant is Excel Medical Products, Inc.. The 510(k) number is K883357.
When did MODEL 1080 ROLLER MASSAGE TABLE receive FDA 510(k) clearance?
MODEL 1080 ROLLER MASSAGE TABLE received FDA 510(k) clearance on 1988-08-23, under 510(k) number K883357.
Who is the listed applicant for MODEL 1080 ROLLER MASSAGE TABLE?
The FDA 510(k) record lists Excel Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 1080 ROLLER MASSAGE TABLE?
The FDA product code for MODEL 1080 ROLLER MASSAGE TABLE is JFB.
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 Excel Medical 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: JFB)
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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