Device Type ID | 4833 |
Device Name | Stains, Microbiologic |
Regulation Description | Dye And Chemical Solution Stains. |
Regulation Medical Specialty | Hematology |
Review Panel | Pathology |
Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
Submission Type | 510(K) Exempt |
CFR Regulation Number | 864.1850 [🔎] |
FDA Device Classification | Class 1 Medical Device |
Product Code | JTS |
GMP Exempt | Yes |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Not Third Party Eligible |
Device Type ID | 4833 |
Device | Stains, Microbiologic |
Product Code | JTS |
FDA Device Classification | Class 1 Medical Device |
Regulation Description | Dye And Chemical Solution Stains. |
CFR Regulation Number | 864.1850 [🔎] |
Recalls | |||
---|---|---|---|
Manufacturer | Recall Class | Date Posted | |
1 | BioMerieux SA | II | Jun-12-2018 |
2 | Remel Inc | II | Nov-25-2014 |