Ri-Star
by Rudolf Riester GmbH & Co. KG
510(k) K932505
Ri-Star is a Class I device made by Rudolf Riester GmbH & Co. KG, cleared under FDA 510(k) K932505 on 8 Oct 1993, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK932505 | Date8 Oct 1993 | StatusActive |
Official records
- FDA 510(k) database K932505
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ERA
- Device class
- Class I
- Regulation
- 21 CFR Part 874.4770
- Advisory committee
- Ear, Nose, Throat
- FDA decision
- SESE Substantially Equivalent
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