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FDA 510(k)

THE ADVANCE SERIES FROM HILL-ROM

K-Number: K922352 · 1992-10-13

ApplicantHill-Rom, Inc.
Decision Date1992-10-13
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE ADVANCE SERIES FROM HILL-ROM 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 1992-10-13 under 510(k) number K922352. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ADVANCE SERIES FROM HILL-ROM?

THE ADVANCE SERIES FROM HILL-ROM is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K922352.

When did THE ADVANCE SERIES FROM HILL-ROM receive FDA 510(k) clearance?

THE ADVANCE SERIES FROM HILL-ROM received FDA 510(k) clearance on 1992-10-13, under 510(k) number K922352.

Who is the listed applicant for THE ADVANCE SERIES FROM HILL-ROM?

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 ADVANCE SERIES FROM HILL-ROM?

The FDA product code for THE ADVANCE SERIES FROM HILL-ROM is FNL.

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Other records listing Hill-Rom, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260211Dashboard (P007000)K202018Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor ActivationK180079Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Packs (different #), Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor ActivationK013709HILL-ROM PRIMAVIEW MONITOR SYSTEMK973705CONTOR TABLE SURFACEK981081BRIGHTSTAR

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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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