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FDA 510(k)

Hair Growth Comb (SZ-23,SZ-23A)

K-Number: K241342 · 2024-11-08

ApplicantShenzhen Nuon Medical Equipment Co., Ltd.
Decision Date2024-11-08
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Hair Growth Comb (SZ-23,SZ-23A) is a medical device manufactured by Shenzhen Nuon Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2024-11-08 under approval number K241342. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Hair Growth Comb (SZ-23,SZ-23A)?

Hair Growth Comb (SZ-23,SZ-23A) is a medical device that received FDA 510(k) clearance on 2024-11-08. It is manufactured by Shenzhen Nuon Medical Equipment Co., Ltd.. The 510(k) number is K241342.

When was Hair Growth Comb (SZ-23,SZ-23A) approved by the FDA?

Hair Growth Comb (SZ-23,SZ-23A) received FDA 510(k) clearance on 2024-11-08, under approval number K241342.

What company makes Hair Growth Comb (SZ-23,SZ-23A)?

Hair Growth Comb (SZ-23,SZ-23A) is manufactured by Shenzhen Nuon Medical Equipment Co., Ltd..

What is the FDA product code for Hair Growth Comb (SZ-23,SZ-23A)?

The FDA product code for Hair Growth Comb (SZ-23,SZ-23A) is OAP.

Other Devices by Shenzhen Nuon Medical Equipment Co., Ltd.

K242700Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-59C, HD-59D, HD-70, HD-72, HD-72A, HD-73A, HD-73B, HD-116, HD-116A, HD-53A, HD-53B) K241155Cold Sore Device (QPZ-03) K251034Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) K242151Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)

Related Devices (Code: OAP)

K162994Capillus302, Capillus312, Capillus352Capillus, LLC K161875LaserCap300, LaserCap224, LaserCap120, LaserCap80Transdermal Cap, Inc. K160728NutraStim Hair Laser HelmetNutra Luxe MD, LLC K161046Laser Helmet LH40-EVOTheradome, Inc. K160285Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202Capillus, LLC K152587DermaScalp Laser CapDermascalp, LLC

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.

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