FDA 510(k)

CHICK/REISON PATIENT EMERG. TROLLEY

K-Number: K834478 · 1984-02-21

ApplicantProfessional Medical Products, Inc.

Decision Date1984-02-21

Product CodeKXJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CHICK/REISON PATIENT EMERG. TROLLEY is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Products, Inc.. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K834478. The device is classified under product code KXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHICK/REISON PATIENT EMERG. TROLLEY?

CHICK/REISON PATIENT EMERG. TROLLEY is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Professional Medical Products, Inc.. The 510(k) number is K834478.

When did CHICK/REISON PATIENT EMERG. TROLLEY receive FDA 510(k) clearance?

CHICK/REISON PATIENT EMERG. TROLLEY received FDA 510(k) clearance on 1984-02-21, under 510(k) number K834478.

Who is the listed applicant for CHICK/REISON PATIENT EMERG. TROLLEY?

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

What is the FDA product code for CHICK/REISON PATIENT EMERG. TROLLEY?

The FDA product code for CHICK/REISON PATIENT EMERG. TROLLEY is KXJ.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Professional Medical Products, Inc. as applicant

K926280STANDARD NEBULIZER HEATER K930270PATIENT PREOPERATIVE PREP TRAY, SINGLE USE K920292VARIOUS KITS AND TRAYS K862010CHICK SURGICAL LIGHT K860739CHICK SURIGICAL LIGHT K830825YIELD NON-ADHERENT DRESSING

View all 9 devices →

Related Devices (Code: KXJ)

K050190APOLLOVilla Sistemi Medicali S.P.A.K963905RADIOGRAPHIC ITT TABLEX-Ray Technologies, Inc.K955414XRT 400Wuestec Medical, Inc.K951146IMAGING TABLESepta Corp.K950068CARBON FIBER COUCH INSERTMedtec, Inc.K950442INFRARED EXPOSURE HAND SWITCHMedical X-Ray Intl., 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.