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FDA 510(k)

HILL-ROM PRIMAVIEW MONITOR SYSTEM

K-Number: K013709 · 2001-11-16

ApplicantHill-Rom, Inc.
Decision Date2001-11-16
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HILL-ROM PRIMAVIEW MONITOR SYSTEM 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 2001-11-16 under 510(k) number K013709. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HILL-ROM PRIMAVIEW MONITOR SYSTEM?

HILL-ROM PRIMAVIEW MONITOR SYSTEM is a medical device that received FDA 510(k) clearance on 2001-11-16. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K013709.

When did HILL-ROM PRIMAVIEW MONITOR SYSTEM receive FDA 510(k) clearance?

HILL-ROM PRIMAVIEW MONITOR SYSTEM received FDA 510(k) clearance on 2001-11-16, under 510(k) number K013709.

Who is the listed applicant for HILL-ROM PRIMAVIEW MONITOR SYSTEM?

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 HILL-ROM PRIMAVIEW MONITOR SYSTEM?

The FDA product code for HILL-ROM PRIMAVIEW MONITOR SYSTEM is FET.

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Other records listing Hill-Rom, Inc. as applicant

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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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