CERVICAL PILLOW— 510(k) K830350

Substantially Equivalent

Deip Enterprises, Inc.

FDA 510(k) clearance K830350 for CERVICAL PILLOW, Substantially Equivalent on 1983-03-09. Applicant: Deip Enterprises, Inc..

Clearance details

Applicant: Deip Enterprises, Inc.
Product code: Code IQK
Advisory panel: Physical Medicine
Date received: 1983-02-03
Decision date: 1983-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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