Bath, Hydro-massage
Penner Patient Care, Inc's record for this product code
Recent MDR events
1 adverse event reports on file
Recalls
10 recall events for this product code
- Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗ - Open, ClassifiedMar 9, 2026
The device does not bear a unique device identifier.
View FDA record ↗
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Penner Patient Care, Inc under this product code.