Atlas FDA

CRYOSTAT

FDA 510(k) clearance K072414 · decided 2008-04-07

Clearance details

K-number
K072414
Device name
CRYOSTAT
Applicant
Lil Drug Store Products, Inc.
Decision
Substantially Equivalent
Date received
2007-08-28
Decision date
2008-04-07
Days to decision
223 days
Clearance type
Traditional
Product code
LKX
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Cedar Rapids, IA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.