Device Type ID | 3364 |
Device Name | Kit, Quality Control For Culture Media |
Regulation Description | Quality Control Kit For Culture Media. |
Regulation Medical Specialty | Microbiology |
Review Panel | Microbiology |
Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
Submission Type | 510(K) Exempt |
CFR Regulation Number | 866.2480 [🔎] |
FDA Device Classification | Class 1 Medical Device |
Product Code | JTR |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Not Third Party Eligible |
Device Type ID | 3364 |
Device | Kit, Quality Control For Culture Media |
Product Code | JTR |
FDA Device Classification | Class 1 Medical Device |
Regulation Description | Quality Control Kit For Culture Media. |
CFR Regulation Number | 866.2480 [🔎] |
Device Problems | |
---|---|
Incorrect, Inadequate Or Imprecise Result Or Readings | 1 |
Total Device Problems | 1 |