THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES— 510(k) K914309
Substantially EquivalentHill-Rom, Inc.
FDA 510(k) clearance K914309 for THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES, Substantially Equivalent on 1992-04-20. Applicant: Hill-Rom, Inc..
Clearance details
- Applicant
- Hill-Rom, Inc.
- Product code
- Code HDD
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Batesville, TN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.