RULER
K-Number: K854892 · 1985-12-24
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Device Summary
Frequently Asked Questions
What is the RULER?
RULER is a medical device that received FDA 510(k) clearance on 1985-12-24. The listed applicant is Euro-Med Intl.. The 510(k) number is K854892.
When did RULER receive FDA 510(k) clearance?
RULER received FDA 510(k) clearance on 1985-12-24, under 510(k) number K854892.
Who is the listed applicant for RULER?
The FDA 510(k) record lists Euro-Med Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RULER?
The FDA product code for RULER is FTY.
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 Euro-Med Intl. 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: FTY)
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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