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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 the device name listed in this FDA 510(k) record. The listed applicant is Kitazato Biopharma Co., Ltd.. It received FDA 510(k) clearance on 2016-04-21 under 510(k) 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. The listed applicant is Kitazato Biopharma Co., Ltd.. The 510(k) number is K160142.

When did MINERAL OIL receive FDA 510(k) clearance?

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

Who is the listed applicant for MINERAL OIL?

The FDA 510(k) record lists Kitazato Biopharma Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINERAL OIL?

The FDA product code for MINERAL OIL is MQL.

Other records listing Kitazato Biopharma Co., Ltd. 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.

Related Devices (Code: MQL)

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.

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.