HERCULITE XR & XRV— 510(k) K943642

Name: FDA 510(k) clearance K943642
Creator: U.S. Food and Drug Administration
Published: 1994-11-17

Substantially Equivalent

Sybron Dental Specialties, Inc.

FDA 510(k) clearance K943642 for HERCULITE XR & XRV, Substantially Equivalent on 1994-11-17. Applicant: Sybron Dental Specialties, Inc.. Device class: 2.

Clearance details

Applicant: Sybron Dental Specialties, Inc.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1994-07-27
Decision date: 1994-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glendora, CA, US

Download summary PDF View on FDA.gov ↗

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