Atlas FDA

ANU ICE

FDA 510(k) clearance K981428 · decided 1998-07-07

Clearance details

K-number
K981428
Device name
ANU ICE
Applicant
Cryoptherapy Pain Relief Products, Inc.
Decision
Substantially Equivalent
Date received
1998-04-20
Decision date
1998-07-07
Days to decision
78 days
Clearance type
Traditional
Product code
LKX
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Pembroke Pines, FL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.