Coburn Optical Ind., Inc.
Coburn Optical Ind., Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1989.
Top product codes for Coburn Optical Ind., Inc.
Recent clearances by Coburn Optical Ind., Inc.
- K892347 — MAGNILINK SYSTEM 101
- K892348 — MAGNILINK SYSTEM 201
- K892349 — MAGNILINK SYSTEM 209
- K892350 — MAGNILINK SYSTEM 402/5
- K892351 — MAGNILINK SYSTEM 602
- K862188 — IRRIGATION & ASPIRATION/VITRECTOMY DEVICE
- K853457 — COBURN I/A SYSTEM
- K821737 — DISP. MICROSURGICAL KNIVES
- K812441 — DI-CROWN
- K803159 — AUTOMATED PERIMETERS
- K801659 — BIOPHTAL CLINICAL ENDOTHELIAL MICROSCOPE
- K801231 — EYE-VAC
- K791659 — MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL
- K781507 — RETINOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.