MICRODAPT DENTAL RESTORATIVE BONDING
K-Number: K830387 · 1983-03-17
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Device Summary
Frequently Asked Questions
What is the MICRODAPT DENTAL RESTORATIVE BONDING?
MICRODAPT DENTAL RESTORATIVE BONDING is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K830387.
When did MICRODAPT DENTAL RESTORATIVE BONDING receive FDA 510(k) clearance?
MICRODAPT DENTAL RESTORATIVE BONDING received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830387.
Who is the listed applicant for MICRODAPT DENTAL RESTORATIVE BONDING?
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 MICRODAPT DENTAL RESTORATIVE BONDING?
The FDA product code for MICRODAPT DENTAL RESTORATIVE BONDING is KLE.
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: KLE)
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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