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FDA 510(k)

WEEVAC 1 PORTABLE RESCUE STRETCHER

K-Number: K902474 · 1990-07-24

ApplicantW. Murphy Ent., Inc.
Decision Date1990-07-24
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WEEVAC 1 PORTABLE RESCUE STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is W. Murphy Ent., Inc.. It received FDA 510(k) clearance on 1990-07-24 under 510(k) number K902474. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEEVAC 1 PORTABLE RESCUE STRETCHER?

WEEVAC 1 PORTABLE RESCUE STRETCHER is a medical device that received FDA 510(k) clearance on 1990-07-24. The listed applicant is W. Murphy Ent., Inc.. The 510(k) number is K902474.

When did WEEVAC 1 PORTABLE RESCUE STRETCHER receive FDA 510(k) clearance?

WEEVAC 1 PORTABLE RESCUE STRETCHER received FDA 510(k) clearance on 1990-07-24, under 510(k) number K902474.

Who is the listed applicant for WEEVAC 1 PORTABLE RESCUE STRETCHER?

The FDA 510(k) record lists W. Murphy Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEEVAC 1 PORTABLE RESCUE STRETCHER?

The FDA product code for WEEVAC 1 PORTABLE RESCUE STRETCHER is FPP.

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 W. Murphy Ent., 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.

K910709WEEVAC TC HAND CARRIED RESCUE STRETCHERK902521WEEVAC 6 INFANT EVACUATION STRETCHER

Related Devices (Code: FPP)

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.

K030283BABY PODPrism Enterprises, Inc.K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, 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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