ANATOM SYSTEM
K-Number: K843233 · 1984-10-25
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Device Summary
Frequently Asked Questions
What is the ANATOM SYSTEM?
ANATOM SYSTEM is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is Lic-Orthion. The 510(k) number is K843233.
When did ANATOM SYSTEM receive FDA 510(k) clearance?
ANATOM SYSTEM received FDA 510(k) clearance on 1984-10-25, under 510(k) number K843233.
Who is the listed applicant for ANATOM SYSTEM?
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 ANATOM SYSTEM?
The FDA product code for ANATOM SYSTEM is KLC.
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: KLC)
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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