Product code HPQ— Ophthalmic

FDA has cleared 5 devices under product code HPQ between 1982 and 1995, filed by 4 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.

• 19952 clearances
• 19862 clearances
• 19821 clearance

• Keeler Instruments, Inc.2 clearances
• Welch Allyn, Inc.1 clearance
• Neitz Instruments Company, Ltd.1 clearance
• Kelleher Corp.1 clearance

• K952289 — WELCH ALLYN FIBER OPTIC HEADLIGNTWelch Allyn, Inc.·1995-07-14
• K951337 — FIBER HEAD LIGHT FH-300Neitz Instruments Company, Ltd.·1995-06-08
• K861746 — KEELER DUAL LIGHTSOURCEKeeler Instruments, Inc.·1986-08-21
• K861747 — KEELER FIBEROPTIC HEADLAMPKeeler Instruments, Inc.·1986-08-21
• K822272 — HEAD MIRRORS W/HEAD LAMPS & HEAD BANDSKelleher Corp.·1982-11-10