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FDA 510(k)

SHASER V-MINI RX

K-Number: K132170 · 2013-11-26

ApplicantShaser, Inc.
Decision Date2013-11-26
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHASER V-MINI RX is the device name listed in this FDA 510(k) record. The listed applicant is Shaser, Inc.. It received FDA 510(k) clearance on 2013-11-26 under 510(k) number K132170. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHASER V-MINI RX?

SHASER V-MINI RX is a medical device that received FDA 510(k) clearance on 2013-11-26. The listed applicant is Shaser, Inc.. The 510(k) number is K132170.

When did SHASER V-MINI RX receive FDA 510(k) clearance?

SHASER V-MINI RX received FDA 510(k) clearance on 2013-11-26, under 510(k) number K132170.

Who is the listed applicant for SHASER V-MINI RX?

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

What is the FDA product code for SHASER V-MINI RX?

The FDA product code for SHASER V-MINI RX is ONF.

Related Clinical Trials

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Other records listing Shaser, Inc. 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.

K132266SHASER HRS2 RX HAIR REMOVAL SYSTEMK130015SHASER V-MINI HAIR REMOVAL SYSTEMK120080SHASER HRS2 HAIR REMOVAL SYSTEMK103560SHASER IPL HAIR REMOVAL SYSTEM

Related Devices (Code: ONF)

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.

K261204Intense Pulsed Light Therapy DeviceSanhe LEFIS Electronics Co., Ltd.K251545Intense Pulsed Light Therapy Device (MMABM-1)Micowey Medical Equipment (Guangxi) Co., Ltd.K231952MEDILIGHTMedicreations, LLCK243123IPL Treatment Device (MDSQMC-01)Medusa (Guangxi)Medical Devices Co., Ltd.K250281DEKA LOTUSEl.En S.P.A.K242440Intense Pulsed Light Treatment System (LK-PT)Nanjing Bestview Laser S&T Co., Ltd.

Official Source

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