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FDA 510(k)

Intraskan DC Plus

K-Number: K170967 · 2017-06-08

ApplicantSkanray Technologies Private Limited
Decision Date2017-06-08
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Intraskan DC Plus is a medical device manufactured by Skanray Technologies Private Limited. It received FDA 510(k) clearance on 2017-06-08 under approval number K170967. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intraskan DC Plus?

Intraskan DC Plus is a medical device that received FDA 510(k) clearance on 2017-06-08. It is manufactured by Skanray Technologies Private Limited. The 510(k) number is K170967.

When was Intraskan DC Plus approved by the FDA?

Intraskan DC Plus received FDA 510(k) clearance on 2017-06-08, under approval number K170967.

What company makes Intraskan DC Plus?

Intraskan DC Plus is manufactured by Skanray Technologies Private Limited.

What is the FDA product code for Intraskan DC Plus?

The FDA product code for Intraskan DC Plus is EHD.

Other Devices by Skanray Technologies Private Limited

K152831Spot Skan K151512Star 60 K170946Skan-C Mobile C-Arm X-Ray System - 230V Variant, Skan-C Mobile C-Arm X-Ray System - 110V Variant

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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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