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)

ERYTHROCYTE & STAND SEDIMENT. RATE TUBE

K-Number: K823761 · 1983-01-21

ApplicantCordis Corp.
Decision Date1983-01-21
Product CodeJPH
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ERYTHROCYTE & STAND SEDIMENT. RATE TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1983-01-21 under 510(k) number K823761. The device is classified under product code JPH. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERYTHROCYTE & STAND SEDIMENT. RATE TUBE?

ERYTHROCYTE & STAND SEDIMENT. RATE TUBE is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Cordis Corp.. The 510(k) number is K823761.

When did ERYTHROCYTE & STAND SEDIMENT. RATE TUBE receive FDA 510(k) clearance?

ERYTHROCYTE & STAND SEDIMENT. RATE TUBE received FDA 510(k) clearance on 1983-01-21, under 510(k) number K823761.

Who is the listed applicant for ERYTHROCYTE & STAND SEDIMENT. RATE TUBE?

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

What is the FDA product code for ERYTHROCYTE & STAND SEDIMENT. RATE TUBE?

The FDA product code for ERYTHROCYTE & STAND SEDIMENT. RATE TUBE is JPH.

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 Cordis 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.

K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

View all 314 devices →

Related Devices (Code: JPH)

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.

K871076WINPETTEUlster Scientific, Inc.K860899DISPETTE IIUlster Scientific, Inc.K852554SRT-SYSTEMMicrowave Development, Inc.K840500SEDIPLASTPrecision Technology, Inc.K831195WESTERGREN DISPETTE FOR ESRUlster Scientific, Inc.K823368DADE ESR KITAmerican Dade

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.

↑