FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Rf/Microwave Hyperthermia, Cancer Treatment

PMA: P820088 · Supplement: S011 · Decision Jun 21, 1990
Classifications
1
FEI Numbers
1
Registration Numbers
1

Basic Information

Device Name
System, Rf/Microwave Hyperthermia, Cancer Treatment
Trade Name
BSD 1000 HYPERTHERMIA SYSTEM
PMA Number
P820088
Supplement Number
S011
Device Class
FDA Class 3
Product Code
LOC
Generic Name
System, rf/microwave hyperthermia, cancer treatment
Medical Specialty
Unknown
Advisory Committee
Radiology
Decision
Approved
Decision Code
APPR
Decision Date
June 21, 1990
Date Received
December 4, 1989
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LOC System, Rf/Microwave Hyperthermia, Cancer Treatment