G. Rodenstock Instrumente GmbH

G. Rodenstock Instrumente GmbH holds 3 FDA 510(k) medical device clearances, first cleared 1986, most recent 1997.

Top product codes for G. Rodenstock Instrumente GmbH

HQF — Ophthalmic2 devices
HLI — Ophthalmic1 device

Recent clearances by G. Rodenstock Instrumente GmbH

K973220 — RODENSTOCK LASER SLITLAMPCode HQF·1997-11-04
K871268 — RODENSTOCK SCANNING LASER OPHTHALMOSCOPECode HLI·1987-06-10
K864063 — ORION 3001, LASER PHOTOCOAGULATORCode HQF·1986-11-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.