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)

DIALYSIS MACHINE, CENTRY II

K-Number: K770857 · 1977-10-04

ApplicantCobe Laboratories, Inc.
Decision Date1977-10-04
Product CodeFJF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIALYSIS MACHINE, CENTRY II is the device name listed in this FDA 510(k) record. The listed applicant is Cobe Laboratories, Inc.. It received FDA 510(k) clearance on 1977-10-04 under 510(k) number K770857. The device is classified under product code FJF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIALYSIS MACHINE, CENTRY II?

DIALYSIS MACHINE, CENTRY II is a medical device that received FDA 510(k) clearance on 1977-10-04. The listed applicant is Cobe Laboratories, Inc.. The 510(k) number is K770857.

When did DIALYSIS MACHINE, CENTRY II receive FDA 510(k) clearance?

DIALYSIS MACHINE, CENTRY II received FDA 510(k) clearance on 1977-10-04, under 510(k) number K770857.

Who is the listed applicant for DIALYSIS MACHINE, CENTRY II?

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

What is the FDA product code for DIALYSIS MACHINE, CENTRY II?

The FDA product code for DIALYSIS MACHINE, CENTRY II is FJF.

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 Cobe Laboratories, Inc. 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.

K923272COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATORK900105COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTICK905793COBE CENTRY 2 BICART OPTION KITK905388COBE CENTRYSYSTEM 3 BICART OPTION KITK904336NEW COBE SATURATION/HEMATOCRIT MONITORK902631COBE ICU CONVERSION KIT

View all 77 devices →

Related Devices (Code: FJF)

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.

K904992MINNILERT AIR DETECTORMinntech Corp.K891327NICKLE-TITANIUM ORTHODONTIC WIREAmerican OrthodonticsK781330BLOOD LEVEL DETECTOR-MODEL 7601Bd Becton Dickinson Vacutainer Systems PreanalyticK780582DETECTOR, BUBBLE & FOAMHospal Medical 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.

↑