BASHAW CERVICAL IMMOBILIZER DEVICE— 510(k) K800108

Name: FDA 510(k) clearance K800108
Creator: U.S. Food and Drug Administration
Published: 1980-02-29

Substantially Equivalent

Bashaw Custom Specialties, Inc.

FDA 510(k) clearance K800108 for BASHAW CERVICAL IMMOBILIZER DEVICE, Substantially Equivalent on 1980-02-29. Applicant: Bashaw Custom Specialties, Inc.. Device class: 1.

Clearance details

Applicant: Bashaw Custom Specialties, Inc.
Product code: Code IQK
Device class: Class 1
Regulation: 21 CFR 890.3490
Advisory panel: Physical Medicine
Date received: 1980-01-16
Decision date: 1980-02-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.