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FDA 510(k)

HILL-ROM PATIENT ENVIRONMENTAL CONTROL SYSTEM

K-Number: K921528 · 1992-04-20

ApplicantHill-Rom, Inc.
Decision Date1992-04-20
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HILL-ROM PATIENT ENVIRONMENTAL CONTROL 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 1992-04-20 under 510(k) number K921528. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HILL-ROM PATIENT ENVIRONMENTAL CONTROL SYSTEM?

HILL-ROM PATIENT ENVIRONMENTAL CONTROL SYSTEM 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 K921528.

When did HILL-ROM PATIENT ENVIRONMENTAL CONTROL SYSTEM receive FDA 510(k) clearance?

HILL-ROM PATIENT ENVIRONMENTAL CONTROL SYSTEM received FDA 510(k) clearance on 1992-04-20, under 510(k) number K921528.

Who is the listed applicant for HILL-ROM PATIENT ENVIRONMENTAL CONTROL 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 PATIENT ENVIRONMENTAL CONTROL SYSTEM?

The FDA product code for HILL-ROM PATIENT ENVIRONMENTAL CONTROL SYSTEM is IQA.

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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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Related Devices (Code: IQA)

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.

K961306DELTATALKER WITH INFRAREDPrentke Romich Co.K953905IMPERIUMTeledyne Brown EngineeringK953937LIAISON COMPUTER ACCESS & ENVIRONMENTAL CONTROL SYSTEMApt Technology, Inc.K943244DEUCEApt Technology, Inc.K944585SCANNING DIRECTORPrentke Romich Co.K944345BEDSIDE BUTLERTrac Medical, Inc.

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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