JUNIPER CLN1 DERMAL COOLING DEVICE— 510(k) K072152

Name: FDA 510(k) clearance K072152
Creator: U.S. Food and Drug Administration
Published: 2007-09-07

Substantially Equivalent

Juniper Medical, Inc.

FDA 510(k) clearance K072152 for JUNIPER CLN1 DERMAL COOLING DEVICE, Substantially Equivalent on 2007-09-07. Applicant: Juniper Medical, Inc.. Device class: 2.

Clearance details

Applicant: Juniper Medical, Inc.
Product code: Code ILO
Device class: Class 2
Regulation: 21 CFR 890.5720
Advisory panel: Physical Medicine
Date received: 2007-08-03
Decision date: 2007-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasanton, CA, US

Download summary PDF View on FDA.gov ↗

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