FDA 510(k)

VIKY UP

K-Number: K122820 · 2013-06-18

Decision Date2013-06-18

Product CodeLKF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

VIKY UP is the device name listed in this FDA 510(k) record. The listed applicant is Endocontrol. It received FDA 510(k) clearance on 2013-06-18 under 510(k) number K122820. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIKY UP?

VIKY UP is a medical device that received FDA 510(k) clearance on 2013-06-18. The listed applicant is Endocontrol. The 510(k) number is K122820.

When did VIKY UP receive FDA 510(k) clearance?

VIKY UP received FDA 510(k) clearance on 2013-06-18, under 510(k) number K122820.

Who is the listed applicant for VIKY UP?

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

What is the FDA product code for VIKY UP?

The FDA product code for VIKY UP is LKF.

Other records listing Endocontrol 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.

K082233VIKY

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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.