FDA 510(k)

Portray

K-Number: K211014 · 2021-07-28

Decision Date2021-07-28

Product CodeEHD

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Portray is the device name listed in this FDA 510(k) record. The listed applicant is Surround Medical Systems. It received FDA 510(k) clearance on 2021-07-28 under 510(k) number K211014. 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 Portray?

Portray is a medical device that received FDA 510(k) clearance on 2021-07-28. The listed applicant is Surround Medical Systems. The 510(k) number is K211014.

When did Portray receive FDA 510(k) clearance?

Portray received FDA 510(k) clearance on 2021-07-28, under 510(k) number K211014.

Who is the listed applicant for Portray?

The FDA 510(k) record lists Surround Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Portray?

The FDA product code for Portray is EHD.

Related Devices (Code: EHD)

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.

K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd.K253864NOMAD Pro 3Dental Imaging Technologies Corporation K252110Dental X-RAY Unit (AJX200)Guangzhou Ajax Medical Equipment Co., Ltd.K254018Portable Dental X-ray Device (GT-1)Guilin Refine Medical Instrument Co., Ltd.K252909Diagnostic X-Ray Equipment Model POCT22Ningbo Runyes Medical Instrument Co., Ltd.K251438Dental X-Ray Device (Ai Ray Lite, Ai Ray Pro, Master Ray )Guilin Woodpecker Medical Instrument Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.