Precision S 4K 0502-655-010
Precision S 4K 0502-655-010 is a Class II device made by Stryker Corp., listed in FDA GUDID since 30 Sep 2019 (UDI-DI 07613327412161), registry data as of 23 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 | Number07613327412161 | Date30 Sep 2019 | StatusListed |
Official records
- AccessGUDID record 07613327412161
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Precision S 4K
- Generic name
- Rigid optical rhinoscope
- Model / Ref / Catalog
- 0502-655-010
- Primary DI / UDI-DI
- 07613327412161
- FDA product code
- EOB
- GMDN term
- Rigid optical rhinoscope
- Device class
- Class II
- Regulation number
- 874.4760
- GUDID distribution status
- In Commercial Distribution
- Size
- Angle — 0.0 degreeLength — 180.0 Millimeter
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