Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)

K-Number: K080300 · 2008-04-08

ApplicantCutera, Inc.
Decision Date2008-04-08
Product CodeNUV
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) is the device name listed in this FDA 510(k) record. The listed applicant is Cutera, Inc.. It received FDA 510(k) clearance on 2008-04-08 under 510(k) number K080300. The device is classified under product code NUV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)?

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) is a medical device that received FDA 510(k) clearance on 2008-04-08. The listed applicant is Cutera, Inc.. The 510(k) number is K080300.

When did CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) receive FDA 510(k) clearance?

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) received FDA 510(k) clearance on 2008-04-08, under 510(k) number K080300.

Who is the listed applicant for CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)?

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

What is the FDA product code for CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)?

The FDA product code for CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) is NUV.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cutera, 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.

K251149AviClear Laser SystemK233237xeo+ FamilyK230660AviClear Laser SystemK223110truSculpt iDK221407truSculpt iDK213461AviClear Laser System

View all 28 devices →

Related Devices (Code: NUV)

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.

K261582Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K231092T-SHAPE 2B&M S.R.L. Marketing Nel BenessereK211272ICOONE Laser Med (also referred to as ICOONE Medical laser)I-Tech Industries SrlK182453ICOONE h (also referred to as ICOONE LASER and ICOONE –h LASER)I-Tech Industries SrlK161892Slimming Treatment DeviceBeijing Honkon Technologies Co., Ltd.K131362INMODE WMBODY DEVICEInmode MD , Ltd.

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.

↑