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.. Device class: 2.
Clearance details
- Applicant
- Hill-Rom, Inc.
- Product code
- Code HDD
- Device class
- Class 2
- Regulation
- 21 CFR 884.4900
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Batesville, TN, US
Recent devices under product code HDD
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Data sourced from openFDA. This site is unofficial and independent of the FDA.