Test, Propoxyphene, Employment And Insurance Testing, Exempt
Device Code: 6270
Product Code(s):
PVI Definition: The Propoxyphene Test Is An In Vitro Diagnostic Test For The Qualitative Analysis Of Propoxyphene For Employment And Insurance Testing. FDA Has Exempted These Devices From The Premarket Notification Requirement By Publishing In The Federal Register O
Device Classification Information
| Device Type ID | 6270 |
| Device Name | Test, Propoxyphene, Employment And Insurance Testing, Exempt |
| Physical State | In Vitro Diagnostic Device |
| Technical Method | Immunoassay |
| Target Area | In Vitro Specimen |
| Regulation Description | Propoxyphene Test System. |
| Regulation Medical Specialty | Toxicology |
| Review Panel | Toxicology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR)
|
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 862.3700 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | PVI |
| GMP Exempt | No |
| Summary MR | Ineligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
Recognized Standards
Total Product Life Cycle
| Device Type ID | 6270 |
| Device | Test, Propoxyphene, Employment And Insurance Testing, Exempt |
| Product Code | PVI |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Propoxyphene Test System. |
| CFR Regulation Number | 862.3700 [🔎] |
TPLC Last Update: 2019-04-02 21:19:39