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FDA 510(k)

WHEELED STRETCHER

K-Number: K961437 · 1996-06-03

ApplicantHill-Rom, Inc.
Decision Date1996-06-03
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WHEELED STRETCHER 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 1996-06-03 under 510(k) number K961437. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELED STRETCHER?

WHEELED STRETCHER is a medical device that received FDA 510(k) clearance on 1996-06-03. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K961437.

When did WHEELED STRETCHER receive FDA 510(k) clearance?

WHEELED STRETCHER received FDA 510(k) clearance on 1996-06-03, under 510(k) number K961437.

Who is the listed applicant for WHEELED STRETCHER?

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 WHEELED STRETCHER?

The FDA product code for WHEELED STRETCHER is FPO.

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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: FPO)

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.

K113598POWER-LOAD COT FASTENER SYSTEMStryker MedicalK072598IRSG I-MOVER FOR BEDSInternational Retail Services Group, LLCK972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)Dyna Corp.K955766ADULT-PEDIATRIC TRANSPORT SYSTEMInternational Biomedical, Inc.K962181HARE MODEL 2000 EZ LOADER MODEL 95555Dyna Corp.K952447HILL-ROM AMBULATORY CARE PROCEDURAL STRETCHERHill-Rom, 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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