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

QUASAR, MODEL MD21

K Number: K032379 · Decision Nov 20, 2003
Classifications
1
FEI Numbers
462
Registration Numbers
462
Same Product Code
228
Applicant Total
1
Review Days
111

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
QUASAR, MODEL MD21
K Number
K032379
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quantum Skincare, Inc.
Date Received
August 1, 2003
Decision Date
November 20, 2003
Product Code
ILY
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ILY Lamp, Infrared, Therapeutic Heating

Similar 510(k) Clearances

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

View all