PILLOWPOSITIVE CERVICAL PILLOW— 510(k) K990871

Name: FDA 510(k) clearance K990871
Creator: U.S. Food and Drug Administration
Published: 1999-06-10

Substantially Equivalent

Lifesleep Systems, Inc.

FDA 510(k) clearance K990871 for PILLOWPOSITIVE CERVICAL PILLOW, Substantially Equivalent on 1999-06-10. Applicant: Lifesleep Systems, Inc.. Device class: 2.

Clearance details

Applicant: Lifesleep Systems, Inc.
Product code: Code MYB
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 1999-03-16
Decision date: 1999-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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