Product code LSB— Physical Medicine

FDA has cleared 4 devices under product code LSB between 1987 and 2001, filed by 3 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 20012 clearances
• 19911 clearance
• 19871 clearance

• Henley Intl.2 clearances
• Thermo-Electric Co.1 clearance
• Chattanooga Group, Inc.1 clearance

• K011768 — THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202Thermo-Electric Co.·2001-08-03
• K011243 — CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000Chattanooga Group, Inc.·2001-07-06
• K896817 — MODEL T11 FLUIDOTHERAPY UNITHenley Intl.·1991-01-18
• K871802 — MODEL K210 AND K211 FLUIDOTHERAPY UNITSHenley Intl.·1987-09-04