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)

IEC CENTRA 4 CENTRIFUGE

K-Number: K821756 · 1982-06-25

ApplicantInternational Equipment Co.
Decision Date1982-06-25
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IEC CENTRA 4 CENTRIFUGE is the device name listed in this FDA 510(k) record. The listed applicant is International Equipment Co.. It received FDA 510(k) clearance on 1982-06-25 under 510(k) number K821756. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IEC CENTRA 4 CENTRIFUGE?

IEC CENTRA 4 CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is International Equipment Co.. The 510(k) number is K821756.

When did IEC CENTRA 4 CENTRIFUGE receive FDA 510(k) clearance?

IEC CENTRA 4 CENTRIFUGE received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821756.

Who is the listed applicant for IEC CENTRA 4 CENTRIFUGE?

The FDA 510(k) record lists International Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IEC CENTRA 4 CENTRIFUGE?

The FDA product code for IEC CENTRA 4 CENTRIFUGE is JQC.

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: JQC)

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.

K183205PureBMC SupraPhysiologic Concentrating System 30 mL System, PureBMC SupraPhysiologic Concentrating System 60 mL System, PureBMC SupraPhysiologic Concentrating System 120 mL SystemEmcyte CorporationK103340SMARTPREP2 BMAC SYSTEM, SMARTPREP PLATELET CONCENTRATION SYSTEMHarvest Technologies, Corp.K081345AXP PLATFORM MARROW XPRESS SYSTEM MODEL 8-5137, 8-5138, 8-5139, 8-5140 (PRIMARY)Thermogenesis Corp.K071934MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KITBiomet Manufacturing CorpK070666GENESISCS COMPONENT CONCENTRATING SYSTEMPerfusion Partners & Assoc., Inc.K052925SMARTPREP2 CENTRIFUGE SYSTEMHarvest Technologies, Corp.

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.

↑