Product code IOB— Physical Medicine

FDA has cleared 6 devices under product code IOB between 1976 and 1991, filed by 6 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.

• 19912 clearances
• 19841 clearance
• 19821 clearance
• 19811 clearance
• 19761 clearance

• Ultralite1 clearance
• Solitec GmbH1 clearance
• Osram GmbH1 clearance
• North American Philips Corp.1 clearance
• Mt. Hood Mfr., Inc.1 clearance
• Dermatron Corp.1 clearance

• K903660 — DERMALIGHT PSORACOMBSolitec GmbH·1991-07-17
• K910091 — ULTRALITE PANELITEUltralite·1991-05-30
• K842276 — SUNMASTERMt. Hood Mfr., Inc.·1984-07-16
• K813451 — UVA FLUORESCENT TANNING LAMPSNorth American Philips Corp.·1982-01-28
• K812853 — OSRAM UVA LAMPOsram GmbH·1981-12-09
• K760519 — SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313Dermatron Corp.·1976-09-03