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FDA 510(k)

PeraServer and PeraTrend

K-Number: K172959 · 2018-05-01

ApplicantPerahealth, Inc.
Decision Date2018-05-01
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PeraServer and PeraTrend is the device name listed in this FDA 510(k) record. The listed applicant is Perahealth, Inc.. It received FDA 510(k) clearance on 2018-05-01 under 510(k) number K172959. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PeraServer and PeraTrend?

PeraServer and PeraTrend is a medical device that received FDA 510(k) clearance on 2018-05-01. The listed applicant is Perahealth, Inc.. The 510(k) number is K172959.

When did PeraServer and PeraTrend receive FDA 510(k) clearance?

PeraServer and PeraTrend received FDA 510(k) clearance on 2018-05-01, under 510(k) number K172959.

Who is the listed applicant for PeraServer and PeraTrend?

The FDA 510(k) record lists Perahealth, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PeraServer and PeraTrend?

The FDA product code for PeraServer and PeraTrend is MWI.

Other records listing Perahealth, Inc. 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.

K183370PeraMobile and PeraWatch

Related Devices (Code: MWI)

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.

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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.

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