LIC-ORTHION MULTI-THERAPY TREATMENT TABLE
K-Number: K862022 · 1986-06-19
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Device Summary
Frequently Asked Questions
What is the LIC-ORTHION MULTI-THERAPY TREATMENT TABLE?
LIC-ORTHION MULTI-THERAPY TREATMENT TABLE is a medical device that received FDA 510(k) clearance on 1986-06-19. The listed applicant is Lic-Orthion. The 510(k) number is K862022.
When did LIC-ORTHION MULTI-THERAPY TREATMENT TABLE receive FDA 510(k) clearance?
LIC-ORTHION MULTI-THERAPY TREATMENT TABLE received FDA 510(k) clearance on 1986-06-19, under 510(k) number K862022.
Who is the listed applicant for LIC-ORTHION MULTI-THERAPY TREATMENT TABLE?
The FDA 510(k) record lists Lic-Orthion as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIC-ORTHION MULTI-THERAPY TREATMENT TABLE?
The FDA product code for LIC-ORTHION MULTI-THERAPY TREATMENT 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 Lic-Orthion 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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