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FDA 510(k)

STRAWBERRY, STRAWBERRY & CREAM

K-Number: K130341 · 2013-09-06

ApplicantLaser Lipo Limited
Decision Date2013-09-06
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRAWBERRY, STRAWBERRY & CREAM is the device name listed in this FDA 510(k) record. The listed applicant is Laser Lipo Limited. It received FDA 510(k) clearance on 2013-09-06 under 510(k) number K130341. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRAWBERRY, STRAWBERRY & CREAM?

STRAWBERRY, STRAWBERRY & CREAM is a medical device that received FDA 510(k) clearance on 2013-09-06. The listed applicant is Laser Lipo Limited. The 510(k) number is K130341.

When did STRAWBERRY, STRAWBERRY & CREAM receive FDA 510(k) clearance?

STRAWBERRY, STRAWBERRY & CREAM received FDA 510(k) clearance on 2013-09-06, under 510(k) number K130341.

Who is the listed applicant for STRAWBERRY, STRAWBERRY & CREAM?

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

What is the FDA product code for STRAWBERRY, STRAWBERRY & CREAM?

The FDA product code for STRAWBERRY, STRAWBERRY & CREAM is OLI.

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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.

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