FOREMOST DENTIN ADHESIVE
K-Number: K845033 · 1985-03-18
Advertisement
Device Summary
Frequently Asked Questions
What is the FOREMOST DENTIN ADHESIVE?
FOREMOST DENTIN ADHESIVE is a medical device that received FDA 510(k) clearance on 1985-03-18. The listed applicant is Foremost Dental Mfg., Inc.. The 510(k) number is K845033.
When did FOREMOST DENTIN ADHESIVE receive FDA 510(k) clearance?
FOREMOST DENTIN ADHESIVE received FDA 510(k) clearance on 1985-03-18, under 510(k) number K845033.
Who is the listed applicant for FOREMOST DENTIN ADHESIVE?
The FDA 510(k) record lists Foremost Dental Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOREMOST DENTIN ADHESIVE?
The FDA product code for FOREMOST DENTIN ADHESIVE is EBF.
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 Foremost Dental Mfg., 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: EBF)
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.
Advertisement