Peritoneal Dialysis System
510(k) K760724
Peritoneal Dialysis System is a Class I device made by Physio-Control Corp., cleared under FDA 510(k) K760724 on 23 Nov 1976, 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 | NumberK760724 | Date23 Nov 1976 | StatusActive |
Official records
- FDA 510(k) database K760724
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EKX
- Device class
- Class I
- Regulation
- 21 CFR Part 872.4200
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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