NPGClass II
Catheter, Infusion, Syringe
21 CFR 870.1210 / Cardiovascular
NPG is the FDA product code for Catheter, Infusion, Syringe, a class II device type, regulated under 21 CFR 870.1210. FDA's definition for this code reads: "To provide physician specified fluids both perivascular or intraluminal to the perivascular space". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.
Classification record
- Product code
- NPG
- Device name
- Catheter, Infusion, Syringe
- FDA definition
- To provide physician specified fluids both perivascular or intraluminal to the perivascular space.
- Regulation
- 21 CFR 870.1210
- Device class
- Class II
- Review panel
- Cardiovascular
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 1
- Ingested recalls
- 0
Clearances, product code NPG
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 2023 | 1 |
Applicants with the most clearances
Product code NPG| Applicant | Clearances |
|---|---|
| Intervene Inc | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeNo registered establishment in MDM’s records lists product code NPG.
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