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FDA 510(k)

Spectralis HRA+OCT and variants with OCT Angiography Module

K-Number: K181594 · 2018-09-13

ApplicantHeidelberg Engineering GmbH
Decision Date2018-09-13
Product CodeOBO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Spectralis HRA+OCT and variants with OCT Angiography Module is the device name listed in this FDA 510(k) record. The listed applicant is Heidelberg Engineering GmbH. It received FDA 510(k) clearance on 2018-09-13 under 510(k) number K181594. The device is classified under product code OBO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Spectralis HRA+OCT and variants with OCT Angiography Module?

Spectralis HRA+OCT and variants with OCT Angiography Module is a medical device that received FDA 510(k) clearance on 2018-09-13. The listed applicant is Heidelberg Engineering GmbH. The 510(k) number is K181594.

When did Spectralis HRA+OCT and variants with OCT Angiography Module receive FDA 510(k) clearance?

Spectralis HRA+OCT and variants with OCT Angiography Module received FDA 510(k) clearance on 2018-09-13, under 510(k) number K181594.

Who is the listed applicant for Spectralis HRA+OCT and variants with OCT Angiography Module?

The FDA 510(k) record lists Heidelberg Engineering GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Spectralis HRA+OCT and variants with OCT Angiography Module?

The FDA product code for Spectralis HRA+OCT and variants with OCT Angiography Module is OBO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07338461High Resolution Imaging OCT StudyRECRUITINGNCT06657716Heidelberg Engineering ANTERION Software Comparison StudyACTIVE_NOT_RECRUITING

Other records listing Heidelberg Engineering GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253837SPECTRALIS HRA+OCT and variants; SPECTRALIS with Flex ModuleK250868SPECTRALIS HRA+OCT and variantsK240924AnterionK241163SPECTRALIS with Flex ModuleK240221SPECTRALIS HRA+OCT and variantsK223557SPECTRALIS HRA+OCT and variants

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Related Devices (Code: OBO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253837SPECTRALIS HRA+OCT and variants; SPECTRALIS with Flex ModuleHeidelberg Engineering GmbHK252633UNITY DX (UDX)Cylite Pty. , Ltd.K250553Tomey Cornea/Anterior Segment OCT (CASIA2)Tomey CorporationK250868SPECTRALIS HRA+OCT and variantsHeidelberg Engineering GmbHK240924AnterionHeidelberg Engineering GmbHK241163SPECTRALIS with Flex ModuleHeidelberg Engineering GmbH

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.

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