JUNIPER CLN1 DERMAL COOLING DEVICE
K-Number: K072152 · 2007-09-07
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Device Summary
Frequently Asked Questions
What is the JUNIPER CLN1 DERMAL COOLING DEVICE?
JUNIPER CLN1 DERMAL COOLING DEVICE is a medical device that received FDA 510(k) clearance on 2007-09-07. The listed applicant is Juniper Medical, Inc.. The 510(k) number is K072152.
When did JUNIPER CLN1 DERMAL COOLING DEVICE receive FDA 510(k) clearance?
JUNIPER CLN1 DERMAL COOLING DEVICE received FDA 510(k) clearance on 2007-09-07, under 510(k) number K072152.
Who is the listed applicant for JUNIPER CLN1 DERMAL COOLING DEVICE?
The FDA 510(k) record lists Juniper Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JUNIPER CLN1 DERMAL COOLING DEVICE?
The FDA product code for JUNIPER CLN1 DERMAL COOLING DEVICE is ILO.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Juniper Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ILO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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