Atlas FDA

ANU-RX

FDA 510(k) clearance K862490 · decided 1986-08-18

Clearance details

K-number
K862490
Device name
ANU-RX
Applicant
J. & Jp., Inc.
Decision
Substantially Equivalent
Date received
1986-07-01
Decision date
1986-08-18
Days to decision
48 days
Clearance type
Traditional
Product code
LKX
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
North Miami Beach, FL, US
Third-party review
No
Expedited review
No

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THERMA-H (K905276)Kure Swiss Medical AG Corp.1991-11-07
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Recalls involving this device

No recalls on record reference this clearance.