SPECTRALIS HRA+OCT and variants
K-Number: K240221 · 2024-07-01
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 2024-07-01. It is manufactured by Heidelberg Engineering GmbH. The 510(k) number is K240221.
When was SPECTRALIS HRA+OCT and variants approved by the FDA?
SPECTRALIS HRA+OCT and variants received FDA 510(k) clearance on 2024-07-01, under approval number K240221.
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.