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FDA 510(k)

PORTABLE ECSCOPE

K-Number: K072353 · 2007-08-30

ApplicantDyansys Corp
Decision Date2007-08-30
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PORTABLE ECSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Dyansys Corp. It received FDA 510(k) clearance on 2007-08-30 under 510(k) number K072353. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE ECSCOPE?

PORTABLE ECSCOPE is a medical device that received FDA 510(k) clearance on 2007-08-30. The listed applicant is Dyansys Corp. The 510(k) number is K072353.

When did PORTABLE ECSCOPE receive FDA 510(k) clearance?

PORTABLE ECSCOPE received FDA 510(k) clearance on 2007-08-30, under 510(k) number K072353.

Who is the listed applicant for PORTABLE ECSCOPE?

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

What is the FDA product code for PORTABLE ECSCOPE?

The FDA product code for PORTABLE ECSCOPE is DPS.

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Related Devices (Code: DPS)

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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