P-10 POSTERIOR FILLING MATERIAL
K-Number: K802751 · 1980-11-12
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Device Summary
Frequently Asked Questions
What is the P-10 POSTERIOR FILLING MATERIAL?
P-10 POSTERIOR FILLING MATERIAL is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is 3M Company. The 510(k) number is K802751.
When did P-10 POSTERIOR FILLING MATERIAL receive FDA 510(k) clearance?
P-10 POSTERIOR FILLING MATERIAL received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802751.
Who is the listed applicant for P-10 POSTERIOR FILLING MATERIAL?
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 P-10 POSTERIOR FILLING MATERIAL?
The FDA product code for P-10 POSTERIOR FILLING MATERIAL is EBH.
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: EBH)
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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