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)

NON INVASIVE VASCULAR PROGRAM

K-Number: K932852 · 1994-02-04

ApplicantD. E. Hokanson, Inc.
Decision Date1994-02-04
Product CodeJOB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NON INVASIVE VASCULAR PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is D. E. Hokanson, Inc.. It received FDA 510(k) clearance on 1994-02-04 under 510(k) number K932852. The device is classified under product code JOB. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON INVASIVE VASCULAR PROGRAM?

NON INVASIVE VASCULAR PROGRAM is a medical device that received FDA 510(k) clearance on 1994-02-04. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K932852.

When did NON INVASIVE VASCULAR PROGRAM receive FDA 510(k) clearance?

NON INVASIVE VASCULAR PROGRAM received FDA 510(k) clearance on 1994-02-04, under 510(k) number K932852.

Who is the listed applicant for NON INVASIVE VASCULAR PROGRAM?

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

What is the FDA product code for NON INVASIVE VASCULAR PROGRAM?

The FDA product code for NON INVASIVE VASCULAR PROGRAM is JOB.

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 D. E. Hokanson, 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.

K041689POLYURETHANE BLOOD PRESSURE CUFFSK033156OB1 OBSTETRICAL DOPPLERK023707A16 BLOOD FLOW MEASUREMENT SYSTEMK982707EC6 PLETHYSMOGRAPHK973426ANS 2000 ECG MONITOR AND RESPIRATION PACERK970570NIVP3 (WINDOWS VERSION OF NIVP

View all 19 devices →

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.

↑