Device Type ID | 5082 |
Device Name | Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat |
Regulation Description | Shortwave Diathermy. |
Regulation Medical Specialty | Physical Medicine |
Review Panel | Physical Medicine |
Premarket Review | Office Of Device Evaluation (ODE) Division Of Neurological And Physical Medicine Devices (DNPMD) Physical Medicine And Rehabilitation Devices Branch (PMDB) |
Submission Type | 510(k) |
CFR Regulation Number | 890.5290 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | ILX |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Not Third Party Eligible |
Device Type ID | 5082 |
Device | Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat |
Product Code | ILX |
FDA Device Classification | Class 2 Medical Device |
Regulation Description | Shortwave Diathermy. |
CFR Regulation Number | 890.5290 [🔎] |