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FDA 510(k)

CRITICAL CARE HOSPITAL BED (ICU/CCU)

K-Number: K915437 · 1992-06-11

ApplicantHill-Rom, Inc.
Decision Date1992-06-11
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CRITICAL CARE HOSPITAL BED (ICU/CCU) 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 1992-06-11 under 510(k) number K915437. 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 CRITICAL CARE HOSPITAL BED (ICU/CCU)?

CRITICAL CARE HOSPITAL BED (ICU/CCU) is a medical device that received FDA 510(k) clearance on 1992-06-11. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K915437.

When did CRITICAL CARE HOSPITAL BED (ICU/CCU) receive FDA 510(k) clearance?

CRITICAL CARE HOSPITAL BED (ICU/CCU) received FDA 510(k) clearance on 1992-06-11, under 510(k) number K915437.

Who is the listed applicant for CRITICAL CARE HOSPITAL BED (ICU/CCU)?

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 CRITICAL CARE HOSPITAL BED (ICU/CCU)?

The FDA product code for CRITICAL CARE HOSPITAL BED (ICU/CCU) 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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Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, 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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