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

invisa-RED ELITE

K Number: K192275 · Decision Aug 19, 2020
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
32
Applicant Total
1
Review Days
363

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
invisa-RED ELITE
K Number
K192275
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
IR Technology, LLC
Date Received
August 22, 2019
Decision Date
August 19, 2020
Product Code
OLI
Advisory Committee
General, Plastic Surgery
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
OLI Fat Reducing Low Level Laser

Similar 510(k) Clearances

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

View all