FOTOFILL DENTAL RESTORATIVE
K-Number: K772279 · 1978-01-03
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Device Summary
Frequently Asked Questions
What is the FOTOFILL DENTAL RESTORATIVE?
FOTOFILL DENTAL RESTORATIVE is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K772279.
When did FOTOFILL DENTAL RESTORATIVE receive FDA 510(k) clearance?
FOTOFILL DENTAL RESTORATIVE received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772279.
Who is the listed applicant for FOTOFILL DENTAL RESTORATIVE?
The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOTOFILL DENTAL RESTORATIVE?
The FDA product code for FOTOFILL DENTAL RESTORATIVE 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 Johnson & Johnson Professionals, 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.
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