MJK — Dna Probe, Trichomonas Vaginalis Class I
FDA product code MJK covers "Dna Probe, Trichomonas Vaginalis", a Class I medical device regulated under 21 CFR 866.2660. Submissions are reviewed by the Microbiology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- MJK
- Device Class
- Class I
- Regulation Number
- 866.2660
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K922457 | microprobe | AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA | September 25, 1992 |