Zoll Pd 5300
510(k) K931787
Zoll Pd 5300 is a Class II device made by Zoll Medical Corp, cleared under FDA 510(k) K931787 on 15 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 | NumberK931787 | Date15 Oct 1993 | StatusActive |
Official records
- FDA 510(k) database K931787
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LDD
- Device class
- Class II
- Regulation
- 21 CFR Part 870.5300
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent