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FDA 510(k)

WEEVAC TC HAND CARRIED RESCUE STRETCHER

K-Number: K910709 · 1991-04-01

ApplicantW. Murphy Ent., Inc.
Decision Date1991-04-01
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WEEVAC TC HAND CARRIED 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 1991-04-01 under 510(k) number K910709. 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 TC HAND CARRIED RESCUE STRETCHER?

WEEVAC TC HAND CARRIED RESCUE STRETCHER is a medical device that received FDA 510(k) clearance on 1991-04-01. The listed applicant is W. Murphy Ent., Inc.. The 510(k) number is K910709.

When did WEEVAC TC HAND CARRIED RESCUE STRETCHER receive FDA 510(k) clearance?

WEEVAC TC HAND CARRIED RESCUE STRETCHER received FDA 510(k) clearance on 1991-04-01, under 510(k) number K910709.

Who is the listed applicant for WEEVAC TC HAND CARRIED 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 TC HAND CARRIED RESCUE STRETCHER?

The FDA product code for WEEVAC TC HAND CARRIED 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.

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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.

K902474WEEVAC 1 PORTABLE 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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