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)

SERVO CART 170

K-Number: K840264 · 1984-02-04

ApplicantSiemens Elema AB
Decision Date1984-02-04
Product CodeBZN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERVO CART 170 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Elema AB. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K840264. The device is classified under product code BZN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVO CART 170?

SERVO CART 170 is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Siemens Elema AB. The 510(k) number is K840264.

When did SERVO CART 170 receive FDA 510(k) clearance?

SERVO CART 170 received FDA 510(k) clearance on 1984-02-04, under 510(k) number K840264.

Who is the listed applicant for SERVO CART 170?

The FDA 510(k) record lists Siemens Elema AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERVO CART 170?

The FDA product code for SERVO CART 170 is BZN.

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 Siemens Elema AB 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.

K023354COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81EK010923KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392EK010925SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407EK002137CATHCOR DESKTOPK001315MODIFICATION TO KION ANESTHESIA SYSTEMK970839SERVO VENTILATOR 300A

View all 63 devices →

Related Devices (Code: BZN)

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.

K924373ACCUFLATE ACCESSORIE CART W/IV POLE AND CLAMPInstrumed, Inc.K872558CART, EMERGENCY, CARDIOPULMONARYNico Metal Products Corp.K850761MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY CMedicor USA , Ltd.K832697RMP INTUBATION EQUIP. STORAGE TRAYRmp Co.K832356PORTABLE OPERAT. RM. MONITORS HS30/40Medtel Pty. , Ltd.K832355CRASH CARTQuinton, 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.

↑