FDA PMA
FDA Class 3
Approved
🇺🇸 United States
System, Rf/Microwave Hyperthermia, Cancer Treatment
PMA: P820088
·
Supplement: S003
·
Decision Oct 29, 1984
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
- S003
- 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
- October 29, 1984
- Date Received
- September 4, 1984
- Expedited Review
- N
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LOC | System, Rf/Microwave Hyperthermia, Cancer Treatment | FDA class 3 | Unknown |