Atlas FDA

WELLHOFER WP700 V. 3.2

FDA 510(k) clearance K945321 · decided 1995-07-12

Clearance details

K-number
K945321
Device name
WELLHOFER WP700 V. 3.2
Applicant
Medical Physics Instrumentation, Inc.
Decision
Substantially Equivalent
Date received
1994-11-01
Decision date
1995-07-12
Days to decision
253 days
Clearance type
Traditional
Product code
IYE
Device class
2
Regulation number
892.5050
Medical specialty
Radiology
Advisory committee
Radiology
Location
Bartlett, TN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2 recall (Z-0683-2016)Iba Dosimetry Gmbh2016-01-21