CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO
K-Number: K831495 · 1983-07-18
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Device Summary
Frequently Asked Questions
What is the CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO?
CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K831495.
When did CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO receive FDA 510(k) clearance?
CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831495.
Who is the listed applicant for CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO?
The FDA 510(k) record lists Scientific Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO?
The FDA product code for CURAY-ECLIPSE VISIBLE LIGHT CURED ORTHO 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 Scientific Pharmaceuticals, 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: 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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