FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FAQ™ (302)

K Number: K242747 · Decision Dec 11, 2024
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
109
Applicant Total
10
Review Days
90

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
FAQ™ (302)
K Number
K242747
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Foreo, Inc.
Date Received
September 12, 2024
Decision Date
December 11, 2024
Product Code
OAP
Advisory Committee
Physical Medicine
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OAP Laser, Comb, Hair

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OAP), ordered by most recent decision date.

View all

Other Clearances by Foreo, Inc.

K Number Device Name
K253683 FAQ™ (LED Panel); FAQ™ (Dual LED Panel)
K241102 Luna 4 plus
K240616 FAQ™ (102)
K232242 BEAR 2 Body
K240378 FAQ™ 201, FAQ™ 202
K231977 PEACH 2, PEACH 2 Duo, PEACH 2 go
K222012 FAQ 101
K200803 BEAR and BEAR mini
K162450 ESPADA Acne-Clearing Blue Light Pen