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

RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM

K Number: K030437 · Decision Apr 10, 2003
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
152
Applicant Total
2
Review Days
59

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
RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM
K Number
K030437
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5650
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Salton, Inc.
Date Received
February 10, 2003
Decision Date
April 10, 2003
Product Code
IRP
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
IRP Massager, Powered Inflatable Tube

Similar 510(k) Clearances

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

View all

Other Clearances by Salton, Inc.

K Number Device Name
K011935 REJUVENIQUE MODEL #RJV10