Product code HOS— Ophthalmic

FDA has cleared 9 devices under product code HOS between 1978 and 1994, filed by 8 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19941 clearance
• 19932 clearances
• 19921 clearance
• 19891 clearance
• 19861 clearance
• 19812 clearances
• 19781 clearance

• Bausch & Lomb, Inc.2 clearances
• Woodlyn, Inc.1 clearance
• R.H. Burton Co.1 clearance
• Mosebach Electric & Supply1 clearance
• Marco Ophthalmic, Inc.1 clearance
• Luneau Ophtalmologie SA1 clearance
• Canon USA, Inc.1 clearance
• American Optical Corp.1 clearance

• K936200 — WIRELESS CHART PROJECTOR,HCP-W 721Canon USA, Inc.·1994-09-28
• K930443 — MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJEMarco Ophthalmic, Inc.·1993-07-06
• K924784 — BURTON PROJECTOR HEAD - MODEL 6000-HR.H. Burton Co.·1993-04-05
• K921214 — OPHTHALMIC PROJECTORLuneau Ophtalmologie SA·1992-06-11
• K890992 — WOODLYN OPHTHALMIC PROJECTORWoodlyn, Inc.·1989-05-17
• K862519 — BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTORBausch & Lomb, Inc.·1986-07-23
• K812706 — MILLER/NADLER GLARE TESTERMosebach Electric & Supply·1981-11-16
• K811180 — ULTRAMATIC PROJECT-O-CHART OPHTH. PROJAmerican Optical Corp.·1981-05-15
• K781658 — PROJECTOR, ACCU-CHART ACUITYBausch & Lomb, Inc.·1978-10-17