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)

ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET

K-Number: K072437 · 2008-02-05

ApplicantRoche Diagnostics
Decision Date2008-02-05
Product CodeNBC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics. It received FDA 510(k) clearance on 2008-02-05 under 510(k) number K072437. The device is classified under product code NBC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET?

ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET is a medical device that received FDA 510(k) clearance on 2008-02-05. The listed applicant is Roche Diagnostics. The 510(k) number is K072437.

When did ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET receive FDA 510(k) clearance?

ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET received FDA 510(k) clearance on 2008-02-05, under 510(k) number K072437.

Who is the listed applicant for ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET?

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

What is the FDA product code for ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET?

The FDA product code for ELECSYS PROBNP II, PRECICONTROL CARDIAC II, PROBNP II CALSET is NBC.

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 Roche Diagnostics 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.

K261686Elecsys Phospho-Tau (217P) PlasmaK252323cobas pulse blood glucose monitoring systemK252280Elecsys Anti-SARS-CoV-2 SK260048Elecsys Anti-HAV IgMK260049Elecsys Anti-HBc IgMK260046Elecsys Anti-HBc II

View all 164 devices →

Related Devices (Code: NBC)

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.

K262109Access NT-proBNPBeckman Coulter, Inc.K252169Access BNP IIBeckman Coulter, Inc.K253539Alere NT-proBNP for Alinity iAxis-Shield Diagnostics, Ltd.K241176Alere NT-proBNP for Alinity i Reagent KitAxis-Shield Diagnostics, Ltd.K232164Access NT-proBNPBeckman Coulter, Inc.K220265ADVIA Centaur® NT-proBNPII (PBNPII)Siemens Healthcare Diagnostics, 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.

↑