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FDA 510(k)

THE PORTABLE ANSISCOPE

K-Number: K071168 · 2007-08-31

ApplicantDyansys, Inc.
Decision Date2007-08-31
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE PORTABLE ANSISCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Dyansys, Inc.. It received FDA 510(k) clearance on 2007-08-31 under 510(k) number K071168. 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 THE PORTABLE ANSISCOPE?

THE PORTABLE ANSISCOPE is a medical device that received FDA 510(k) clearance on 2007-08-31. The listed applicant is Dyansys, Inc.. The 510(k) number is K071168.

When did THE PORTABLE ANSISCOPE receive FDA 510(k) clearance?

THE PORTABLE ANSISCOPE received FDA 510(k) clearance on 2007-08-31, under 510(k) number K071168.

Who is the listed applicant for THE PORTABLE ANSISCOPE?

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

What is the FDA product code for THE PORTABLE ANSISCOPE?

The FDA product code for THE PORTABLE ANSISCOPE is DPS.

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Other records listing Dyansys, 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.

K221425Primary ReliefK221231Drug Relief v1K220397ANSiStim-PPK213188Primary ReliefK212859First ReliefK211971Drug Relief v1

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Related Devices (Code: DPS)

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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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