Spectralis HRA+OCT and Variants
K-Number: K192391 · 2019-09-26
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 2019-09-26. It is manufactured by Heidelberg Engineering GmbH. The 510(k) number is K192391.
When was Spectralis HRA+OCT and Variants approved by the FDA?
Spectralis HRA+OCT and Variants received FDA 510(k) clearance on 2019-09-26, under approval number K192391.
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.