LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00— 510(k) K990212

Name: FDA 510(k) clearance K990212
Creator: U.S. Food and Drug Administration
Published: 1999-09-14

Substantially Equivalent

Doctor'S Research Group, Inc.

FDA 510(k) clearance K990212 for LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00, Substantially Equivalent on 1999-09-14. Applicant: Doctor'S Research Group, Inc.. Device class: 2.

Clearance details

Applicant: Doctor'S Research Group, Inc.
Product code: Code DYX
Device class: Class 2
Regulation: 21 CFR 872.4600
Advisory panel: Dental
Date received: 1999-01-22
Decision date: 1999-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wolcott, CT, US

Download summary PDF View on FDA.gov ↗

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