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)

EMERGENCY/ACCIDENT TROLLEY 550

K-Number: K946101 · 1995-02-07

ApplicantHogan & Hartson
Decision Date1995-02-07
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EMERGENCY/ACCIDENT TROLLEY 550 is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K946101. 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 EMERGENCY/ACCIDENT TROLLEY 550?

EMERGENCY/ACCIDENT TROLLEY 550 is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is Hogan & Hartson. The 510(k) number is K946101.

When did EMERGENCY/ACCIDENT TROLLEY 550 receive FDA 510(k) clearance?

EMERGENCY/ACCIDENT TROLLEY 550 received FDA 510(k) clearance on 1995-02-07, under 510(k) number K946101.

Who is the listed applicant for EMERGENCY/ACCIDENT TROLLEY 550?

The FDA 510(k) record lists Hogan & Hartson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERGENCY/ACCIDENT TROLLEY 550?

The FDA product code for EMERGENCY/ACCIDENT TROLLEY 550 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 Hogan & Hartson 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.

K974168COOPERSURGICAL INFRARED COAGULATORK973849BIOABSORBABLE BANKART TACKK973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEK950169RIBOSOMAL P EIA TEST SYSTEMK942389TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVESK946217CARDIOLIPIN M EIA TEST SYSTEM

View all 26 devices →

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.

↑