Product code HMG— Ophthalmic

FDA has cleared 4 devices under product code HMG between 1984 and 1990, filed by 4 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.

• 19901 clearance
• 19881 clearance
• 19871 clearance
• 19841 clearance

• Woodlyn, Inc.1 clearance
• Site Microsurgical Systems, Inc.1 clearance
• Jedmed Instrument Co.1 clearance
• Gorsk, Inc.1 clearance

• K900161 — A-SCAN ROLL-AROUND STANDJedmed Instrument Co.·1990-02-16
• K883575 — MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USESite Microsurgical Systems, Inc.·1988-09-12
• K873554 — GORSK INSTRUMENT RESTGorsk, Inc.·1987-10-23
• K841759 — OPHTHALMIC TABLEWoodlyn, Inc.·1984-06-01