DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE— 510(k) K842788

Name: FDA 510(k) clearance K842788
Creator: U.S. Food and Drug Administration
Published: 1984-09-11

Substantially Equivalent

Brimms, Inc.

FDA 510(k) clearance K842788 for DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE, Substantially Equivalent on 1984-09-11. Applicant: Brimms, Inc.. Device class: 2.

Clearance details

Applicant: Brimms, Inc.
Product code: Code JXL
Device class: Class 2
Regulation: 21 CFR 882.5070
Advisory panel: Neurology
Date received: 1984-07-23
Decision date: 1984-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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