Heidelberg Engineering
Heidelberg Engineering holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2010, with 1 FDA device recall on record.
Top product codes for Heidelberg Engineering
FDA recalls by Heidelberg Engineering
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Heidelberg Engineering
- K101223 — SPECTRALIS HRA+OCT, SPECTRALIS FA_OCT, SPECTRALIS ICGA+ OCT, SPECTRALIS HRA, SPECTRALIS FA
- K063191 — HEIDELBERG RETINA ANGIOGRAPH 2/OPTICAL COHERENCE TOMOGRAPH, MODEL HRA 2/OCT
- K052935 — HEIDELBERG ENGINEERING SLITLAMP-OCT (SL-OCT)
- K042742 — HEIDELBERG RETINA TOMOGRAPH II / ROSTOCK CORNEA MODULE (HRT II / RCM)
- K971671 — HEIDELBERG RETINA ANGIOGRAPH FA/ICGA (HRA/C)
- K943955 — RETINA FLOWMETER
- K943956 — RETINA TOMOGRAPH AND FLOWMETER
- K944261 — RETINA ANGIOGRAPH
- K912891 — HEIDELBERG RETINA TOMOGRAPH
Data sourced from openFDA. This site is unofficial and independent of the FDA.