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FDA 510(k)

PAD, HOSPITAL STRETCHER

K-Number: K801935 · 1980-08-27

ApplicantVolunteer Blind Industries, Inc.
Decision Date1980-08-27
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PAD, HOSPITAL STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Volunteer Blind Industries, Inc.. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801935. 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 PAD, HOSPITAL STRETCHER?

PAD, HOSPITAL STRETCHER is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Volunteer Blind Industries, Inc.. The 510(k) number is K801935.

When did PAD, HOSPITAL STRETCHER receive FDA 510(k) clearance?

PAD, HOSPITAL STRETCHER received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801935.

Who is the listed applicant for PAD, HOSPITAL STRETCHER?

The FDA 510(k) record lists Volunteer Blind Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAD, HOSPITAL STRETCHER?

The FDA product code for PAD, HOSPITAL STRETCHER is FPO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Volunteer Blind Industries, 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.

K801936PAD, EXAMINING TABLE

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.K961437WHEELED 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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