ORTHODONTIC. PLASTIC BRACKET PRIMER
K-Number: K780028 · 1978-01-17
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Device Summary
Frequently Asked Questions
What is the ORTHODONTIC. PLASTIC BRACKET PRIMER?
ORTHODONTIC. PLASTIC BRACKET PRIMER is a medical device that received FDA 510(k) clearance on 1978-01-17. The listed applicant is 3M Company. The 510(k) number is K780028.
When did ORTHODONTIC. PLASTIC BRACKET PRIMER receive FDA 510(k) clearance?
ORTHODONTIC. PLASTIC BRACKET PRIMER received FDA 510(k) clearance on 1978-01-17, under 510(k) number K780028.
Who is the listed applicant for ORTHODONTIC. PLASTIC BRACKET PRIMER?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ORTHODONTIC. PLASTIC BRACKET PRIMER?
The FDA product code for ORTHODONTIC. PLASTIC BRACKET 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 3M Company 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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