RELIANCE METAL PRIMER
K-Number: K880766 · 1988-04-25
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Device Summary
Frequently Asked Questions
What is the RELIANCE METAL PRIMER?
RELIANCE METAL PRIMER is a medical device that received FDA 510(k) clearance on 1988-04-25. The listed applicant is Reliance Orthodontic Products, Inc.. The 510(k) number is K880766.
When did RELIANCE METAL PRIMER receive FDA 510(k) clearance?
RELIANCE METAL PRIMER received FDA 510(k) clearance on 1988-04-25, under 510(k) number K880766.
Who is the listed applicant for RELIANCE METAL PRIMER?
The FDA 510(k) record lists Reliance Orthodontic Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RELIANCE METAL PRIMER?
The FDA product code for RELIANCE METAL PRIMER 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 Reliance Orthodontic Products, 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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