Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
FDA product code ILX · 15 cleared devices
Class 2
Physical Medicine
- Regulation
- 21 CFR 890.5290
- Review panel
- PM
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1989-04-27 – 2024-12-18
ILX
2024-12-18
ILX
2020-12-15
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2019-06-28
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2013-12-13
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2013-05-06
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ILX
2012-07-27
ZEOBI
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2010-04-07
PROVANT SYSTEM, MODEL 4201
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ILX
2009-12-18
ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE
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ILX
2009-12-15
ORTHOCOR KNEE SYSTEM BASIC
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ILX
2008-12-11
IVIVI SOFPULSE, MODELS 912-M10, ROMA3 AND TORINO II
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ILX
2007-05-24
MODEL PMT850
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ILX
2002-08-08
ACTIBAND
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ILX
1997-10-21
REGENESIS MODEL 42
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ILX
1991-01-17
MAGNETIC RESONANCE THERAPY DEVICE
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ILX
1989-04-27
PULSAR EM
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