Cleared Traditional

K141567 - IGROW - II HAIR GROWTH SYSTEM, IGROW HAIR GROWTH SYSTEM

K141567 is an FDA 510(k) clearance for IGROW - II HAIR GROWTH SYSTEM, manufactured by Apira Science, Inc.. The device is a Class 2 General & Plastic Surgery device with product code OAP cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K141567 · Apira Science, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2014
Decision
70d
Days
Class 2
Risk

K141567 is an FDA 510(k) clearance for the IGROW - II HAIR GROWTH SYSTEM, IGROW HAIR GROWTH SYSTEM. Classified as Laser, Comb, Hair (product code OAP), Class II - Special Controls.

Submitted by Apira Science, Inc. (Chatham, US). The FDA issued a Cleared decision on August 21, 2014 after a review of 70 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 890.5500 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Apira Science, Inc. devices

FDA 510(k) Submission Details - K141567

510(k) Number K141567 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 12, 2014
Decision Date August 21, 2014
Days to Decision 70 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 115d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OAP Device Classification - Class 2, Special Controls

Product Code OAP Laser, Comb, Hair
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5500
Definition Promote Hair Growth In Males With Androgenic Alopecia And Norwood Hamilton Classification Of Iia To V
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - OAP Laser, Comb, Hair

All 113
Devices cleared under the same product code (OAP) and FDA review panel - the closest regulatory comparables to K141567.
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K142573 · Lexington International, LLC · Dec 2014
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LASERBRUSH
K121920 · Sunetics International Marketing Group, LLC · Jun 2013
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K122950 · Theradome, Inc. · Jun 2013