ORTHO LIGHT CURE
K-Number: K913854 · 1992-01-14
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Device Summary
Frequently Asked Questions
What is the ORTHO LIGHT CURE?
ORTHO LIGHT CURE is a medical device that received FDA 510(k) clearance on 1992-01-14. The listed applicant is Ortho Source. The 510(k) number is K913854.
When did ORTHO LIGHT CURE receive FDA 510(k) clearance?
ORTHO LIGHT CURE received FDA 510(k) clearance on 1992-01-14, under 510(k) number K913854.
Who is the listed applicant for ORTHO LIGHT CURE?
The FDA 510(k) record lists Ortho Source as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ORTHO LIGHT CURE?
The FDA product code for ORTHO LIGHT CURE is DYH.
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 Ortho Source 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: DYH)
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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