Spectralis HRA+OCT and variants
K-Number: K201252 · 2020-09-09
Device Summary
Frequently Asked Questions
What is the Spectralis HRA+OCT and variants?
Spectralis HRA+OCT and variants is a medical device that received FDA 510(k) clearance on 2020-09-09. It is manufactured by Heidelberg Engineering GmbH. The 510(k) number is K201252.
When was Spectralis HRA+OCT and variants approved by the FDA?
Spectralis HRA+OCT and variants received FDA 510(k) clearance on 2020-09-09, under approval number K201252.
What company makes Spectralis HRA+OCT and variants?
Spectralis HRA+OCT and variants is manufactured by Heidelberg Engineering GmbH.
What is the FDA product code for Spectralis HRA+OCT and variants?
The FDA product code for Spectralis HRA+OCT and variants is OBO.
Other Devices by Heidelberg Engineering GmbH
Related Devices (Code: OBO)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.