HYBRID DENTAL PRODUCT— 510(k) K813550

Substantially Equivalent

Dentsply Intl.

FDA 510(k) clearance K813550 for HYBRID DENTAL PRODUCT, Substantially Equivalent on 1982-02-24. Applicant: Dentsply Intl.. Device class: 1.

Clearance details

Applicant: Dentsply Intl.
Product code: Code EBH
Device class: Class 1
Regulation: 21 CFR 872.3670
Advisory panel: Dental
Date received: 1981-12-21
Decision date: 1982-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.