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)

NUTRITONE FACIAL BEAUTY SYSTEM

K-Number: K070250 · 2008-09-04

ApplicantIsomers Laboratories, Inc.
Decision Date2008-09-04
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NUTRITONE FACIAL BEAUTY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Isomers Laboratories, Inc.. It received FDA 510(k) clearance on 2008-09-04 under 510(k) number K070250. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUTRITONE FACIAL BEAUTY SYSTEM?

NUTRITONE FACIAL BEAUTY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-09-04. The listed applicant is Isomers Laboratories, Inc.. The 510(k) number is K070250.

When did NUTRITONE FACIAL BEAUTY SYSTEM receive FDA 510(k) clearance?

NUTRITONE FACIAL BEAUTY SYSTEM received FDA 510(k) clearance on 2008-09-04, under 510(k) number K070250.

Who is the listed applicant for NUTRITONE FACIAL BEAUTY SYSTEM?

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

What is the FDA product code for NUTRITONE FACIAL BEAUTY SYSTEM?

The FDA product code for NUTRITONE FACIAL BEAUTY SYSTEM is NFO.

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

Related Devices (Code: NFO)

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.

K261370LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA))Guangdong Newdermo Biotech Co., Ltd.K262861PureLift Pro MaxXtreem Pulse, LLCK260387SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)Hironic Co., Ltd.K253932FACEGYM Pro Device (HD-109)Shenzhen Kaiyan Medical Equipment Co., Ltd.K260179VITA Multi-Function Head Brush (TB-2343F, TB-2442F)Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.K260895Ulike Clear Zero (YC10 BU)Guangxi Ulike Medical Technology Co., 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.

↑