Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EVACU-SLED

K-Number: K940245 · 1994-02-28

ApplicantEvacu Technologies, Inc.
Decision Date1994-02-28
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EVACU-SLED is the device name listed in this FDA 510(k) record. The listed applicant is Evacu Technologies, Inc.. It received FDA 510(k) clearance on 1994-02-28 under 510(k) number K940245. 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 EVACU-SLED?

EVACU-SLED is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Evacu Technologies, Inc.. The 510(k) number is K940245.

When did EVACU-SLED receive FDA 510(k) clearance?

EVACU-SLED received FDA 510(k) clearance on 1994-02-28, under 510(k) number K940245.

Who is the listed applicant for EVACU-SLED?

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

What is the FDA product code for EVACU-SLED?

The FDA product code for EVACU-SLED 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

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.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, Inc.K924669FERNO-WASHINGTON BASKET STRETCHER, MODEL 71-WFerno

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.

↑