Pathway® 6330
by Prometheus Group of New Hampshire Limited, the
Pathway® 6330 is a Class II device made by Prometheus Group of New Hampshire Limited, the, listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00852423006172), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00852423006172 | Date26 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00852423006172
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pathway®
- Generic name
- Perineometer
- Model / Ref / Catalog
- 6330
- Primary DI / UDI-DI
- 00852423006172
- FDA product code
- KPI
- GMDN term
- Perineometer
- Device class
- Class II
- Regulation number
- 876.5320
- GUDID distribution status
- In Commercial Distribution
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