KIY — Chamber, Slide Culture Class I
FDA product code KIY covers "Chamber, Slide Culture", a Class I medical device regulated under 21 CFR 864.2240. 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
- KIY
- Device Class
- Class I
- Regulation Number
- 864.2240
- Submission Type
- Review Panel
- PA
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K781516 | zeus scientific | TEST SYSTEM TISSUE CELL CULTURE SLIDE | September 27, 1978 |