UNIVERSAL BITE BLOCK— 510(k) K960663

Name: FDA 510(k) clearance K960663
Creator: U.S. Food and Drug Administration
Published: 1996-05-17

Substantially Equivalent

B&B Medical Technologies, Inc.

FDA 510(k) clearance K960663 for UNIVERSAL BITE BLOCK, Substantially Equivalent on 1996-05-17. Applicant: B&B Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: B&B Medical Technologies, Inc.
Product code: Code JXL
Device class: Class 2
Regulation: 21 CFR 882.5070
Advisory panel: Neurology
Date received: 1996-02-16
Decision date: 1996-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangevale, CA, US

Download summary PDF View on FDA.gov ↗

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