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FDA 510(k)

MINERAL OIL

K-Number: K160142 · 2016-04-21

Decision Date2016-04-21
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINERAL OIL is a medical device manufactured by Kitazato Biopharma Co., Ltd.. It received FDA 510(k) clearance on 2016-04-21 under approval number K160142. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINERAL OIL?

MINERAL OIL is a medical device that received FDA 510(k) clearance on 2016-04-21. It is manufactured by Kitazato Biopharma Co., Ltd.. The 510(k) number is K160142.

When was MINERAL OIL approved by the FDA?

MINERAL OIL received FDA 510(k) clearance on 2016-04-21, under approval number K160142.

What company makes MINERAL OIL?

MINERAL OIL is manufactured by Kitazato Biopharma Co., Ltd..

What is the FDA product code for MINERAL OIL?

The FDA product code for MINERAL OIL is MQL.

Other Devices by Kitazato Biopharma Co., Ltd.

Related Devices (Code: MQL)

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.