PAROJECT ANESTHETIC SYRINGE— 510(k) K904279

Name: FDA 510(k) clearance K904279
Creator: U.S. Food and Drug Administration
Published: 1990-12-07

Substantially Equivalent

Ronvig Instruments, Ltd.

FDA 510(k) clearance K904279 for PAROJECT ANESTHETIC SYRINGE, Substantially Equivalent on 1990-12-07. Applicant: Ronvig Instruments, Ltd.. Device class: 2.

Clearance details

Applicant: Ronvig Instruments, Ltd.
Product code: Code EGM
Device class: Class 2
Regulation: 21 CFR 872.4475
Advisory panel: Dental
Date received: 1990-09-17
Decision date: 1990-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milford, DE, US

Download summary PDF View on FDA.gov ↗

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