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FDA 510(k)

Flip Lube

K-Number: K171516 · 2018-02-05

ApplicantImquest Biosciences, Inc.
Decision Date2018-02-05
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Flip Lube is a medical device manufactured by Imquest Biosciences, Inc.. It received FDA 510(k) clearance on 2018-02-05 under approval number K171516. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Flip Lube?

Flip Lube is a medical device that received FDA 510(k) clearance on 2018-02-05. It is manufactured by Imquest Biosciences, Inc.. The 510(k) number is K171516.

When was Flip Lube approved by the FDA?

Flip Lube received FDA 510(k) clearance on 2018-02-05, under approval number K171516.

What company makes Flip Lube?

Flip Lube is manufactured by Imquest Biosciences, Inc..

What is the FDA product code for Flip Lube?

The FDA product code for Flip Lube is NUC.

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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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