Micro Guide Catheter Xp
by Cordis Corp.
510(k) K082143
Micro Guide Catheter Xp is a Class II device made by Cordis Corp., cleared under FDA 510(k) K082143 on 25 Aug 2008, active as of 11 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 | NumberK082143 | Date25 Aug 2008 | StatusActive |
Official records
- FDA 510(k) database K082143
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- PDU
- Device class
- Class II
- Regulation
- 21 CFR Part 870.1250
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent
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