KIQ — Kit, Culture, Chromosome Class I
FDA product code KIQ covers "Kit, Culture, Chromosome", a Class I medical device regulated under 21 CFR 864.2260. Submissions are reviewed by the Hematology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- KIQ
- Device Class
- Class I
- Regulation Number
- 864.2260
- Submission Type
- Review Panel
- PA
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K790239 | pharmacia fine chemicals | PHYTOHAEMAGGLUTININ | March 8, 1979 |