Device Type ID | 2354 |
Device Name | Blood, Occult, Enzymatic Method, In Urine |
Regulation Description | Occult Blood Test. |
Regulation Medical Specialty | Hematology |
Review Panel | Hematology |
Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
Submission Type | 510(k) |
CFR Regulation Number | 864.6550 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | JIP |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Eligible For Accredited Persons Program |
Device Type ID | 2354 |
Device | Blood, Occult, Enzymatic Method, In Urine |
Product Code | JIP |
FDA Device Classification | Class 2 Medical Device |
Regulation Description | Occult Blood Test. |
CFR Regulation Number | 864.6550 [🔎] |