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FDA 510(k)

THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES

K-Number: K914309 · 1992-04-20

ApplicantHill-Rom, Inc.
Decision Date1992-04-20
Product CodeHDD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom, Inc.. It received FDA 510(k) clearance on 1992-04-20 under 510(k) number K914309. The device is classified under product code HDD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES?

THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES is a medical device that received FDA 510(k) clearance on 1992-04-20. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K914309.

When did THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES receive FDA 510(k) clearance?

THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES received FDA 510(k) clearance on 1992-04-20, under 510(k) number K914309.

Who is the listed applicant for THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES?

The FDA 510(k) record lists Hill-Rom, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES?

The FDA product code for THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES is HDD.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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