GRZ — Antisera, Fluorescent, All, Mycoplasma Spp. Class I
FDA Device Classification
Classification Details
- Product Code
- GRZ
- Device Class
- Class I
- Regulation Number
- 866.3375
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K946373 | zeus scientific | MYCOPLASMA SLURRY AND MYCOPLASMA CROWNTITRE IFA TEST SYSTEM | February 7, 1996 |
| K944417 | zeus scientific | ZEUA MYCOPLASMA | August 1, 1995 |
| K931557 | fuller laboratories | FULLER LABORATORIES MYCOPLASM PNEUMONIA IFA-IGG TEST | March 11, 1994 |
| K861716 | whittaker bioproducts | FIAX TEST KIT FOR MYCOPLASMA PNEUMONIAE-G ANTIBODY | August 8, 1986 |
| K840012 | zeus technologies | INDIRECT FLUORESCENT ANTIBODY MYCO | February 27, 1984 |