Product code HOH— Ophthalmic

FDA has cleared 3 devices under product code HOH between 1981 and 1994, filed by 3 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
• 19881 clearance
• 19811 clearance

• Seiler Instrument & Mfg. Co., Inc.1 clearance
• General Scientific Corp.1 clearance
• Exeter Instruments, Inc.1 clearance

• K934494 — SURGITELGeneral Scientific Corp.·1994-01-25
• K875124 — LOW-POWER BINOCULAR LOUPESeiler Instrument & Mfg. Co., Inc.·1988-02-19
• K810817 — EXETER OPERATING LOUPEExeter Instruments, Inc.·1981-04-23