510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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PASHumanitarian device exemption

Rf/Microwave Hyperthermia System, Cancer Treatment

Unknown
FDA source (opens on fda.gov)

PAS is the FDA product code for Rf/Microwave Hyperthermia System, Cancer Treatment. FDA's definition for this code reads: "Used in conjunction with radiation therapy for the treatment of cervical carcinoma patients who normally would be treated with combined chemotherapy and radiation but are ineligible for chemotherapy due to patient related factors". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
PAS
Device name
Rf/Microwave Hyperthermia System, Cancer Treatment
FDA definition
Used in conjunction with radiation therapy for the treatment of cervical carcinoma patients who normally would be treated with combined chemotherapy and radiation but are ineligible for chemotherapy due to patient related factors.
Device class
Humanitarian device exemption
Review panel
Unknown
Submission type
FDA code 6
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code PAS.