FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

JUNIPER CLN1 DERMAL COOLING DEVICE

K Number: K072152 · Decision Sep 7, 2007
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
2
Review Days
35

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
JUNIPER CLN1 DERMAL COOLING DEVICE
K Number
K072152
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Juniper Medical, Inc.
Date Received
August 3, 2007
Decision Date
September 7, 2007
Product Code
ILO
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ILO Pack, Hot Or Cold, Water Circulating

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ILO), ordered by most recent decision date.

View all

Other Clearances by Juniper Medical, Inc.

K Number Device Name
K063715 JUNIPER COOLING DEVICE XTRA