FDA 510(k) Applications for Medical Device Product Code "LSB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K011243 | CHATTANOOGA GROUP, INC. | CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000 | 07/06/2001 |
K011768 | THERMO-ELECTRIC CO. | THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202 | 08/03/2001 |