Heine Optotechnik GmbH & Co. KG
Heine Optotechnik GmbH & Co. KG holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2015.
Top product codes for Heine Optotechnik GmbH & Co. KG
Recent clearances by Heine Optotechnik GmbH & Co. KG
- K142486 — HEINE BETA 200, HEINE BETA 200 S, HEINE K 180
- K142837 — HEINE SIGMA 250 & HEINE SIGMA 250 M2
- K131959 — HEINE MINI 3000(R) OPHTHALMOSCOPE
- K131961 — HEINE BETA 200(R) OPHTHALMOSCOPE
- K123587 — HEINE MINI 3000 LED OPHTHALMOSCOPE
- K123316 — HEINE OMEGA 500
- K101892 — HEINE GAMMA G7; HEINE GAMMA G5, HEINE GAMMA GP, HEINE GAMMA GST, HEINE GAMMA XXL LF MODEL M-000.09.23X, M-000.09.24X, M-
Data sourced from openFDA. This site is unofficial and independent of the FDA.