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 CART

K-Number: K772320 · 1978-01-03

ApplicantPhysio-Control Corp.
Decision Date1978-01-03
Product CodeBZN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMERGENCY CART is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772320. 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 EMERGENCY CART?

EMERGENCY CART is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Physio-Control Corp.. The 510(k) number is K772320.

When did EMERGENCY CART receive FDA 510(k) clearance?

EMERGENCY CART received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772320.

Who is the listed applicant for EMERGENCY CART?

The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERGENCY CART?

The FDA product code for EMERGENCY CART 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 Physio-Control Corp. 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.

K991910LIFEPAK 12 BIPHASICK990338NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEMK983393LIFEPAK 500 BIPHASICK973486LIFE PAK 12K962359LIFEPAK 300K955854LIFEPAK 500

View all 80 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.K840264SERVO CART 170Siemens Elema ABK832697RMP INTUBATION EQUIP. STORAGE TRAYRmp Co.K832356PORTABLE OPERAT. RM. MONITORS HS30/40Medtel Pty. , Ltd.

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.

↑