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)

ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE

K-Number: K874020 · 1988-01-29

ApplicantAbbott Laboratories
Decision Date1988-01-29
Product CodeKPF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1988-01-29 under 510(k) number K874020. The device is classified under product code KPF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE?

ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Abbott Laboratories. The 510(k) number is K874020.

When did ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE receive FDA 510(k) clearance?

ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE received FDA 510(k) clearance on 1988-01-29, under 510(k) number K874020.

Who is the listed applicant for ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE?

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

What is the FDA product code for ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE?

The FDA product code for ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE is KPF.

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 Abbott Laboratories 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.

K262156Anti-HCV NextK252424Anti-HCV NextK243500ARCHITECT iGentamicinK243168Alinity i Rubella IgGK243283Alinity h-series SystemK233932Alinity i Toxo IgM

View all 876 devices →

Related Devices (Code: KPF)

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.

K061515RENALSOFTBaxter Healthcare CorpK990953RENAL LINKBaxter Healthcare CorpK970989CYBERRENCybernius Medical , Ltd.K955762PACKPD PERITONEAL DIALYSIS UREA KINETIC MODELING SOFTWARE PROGRAMFresenius USA, Inc.K913515TOTAL CONTAINMENT DEVICEDencoK875121AMICON EQUALINE FLUID BALANCE SYSTEMAmicon, 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.

↑