LPW — System, Test, Oxalate Class I
FDA product code LPW covers "System, Test, Oxalate", a Class I medical device regulated under 21 CFR 862.1542. Submissions are reviewed by the Clinical Chemistry panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LPW
- Device Class
- Class I
- Regulation Number
- 862.1542
- Submission Type
- Review Panel
- CH
- Medical Specialty
- Clinical Chemistry
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K883525 | sigma chemical | OXALATE REAGENT | October 25, 1988 |