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)

BEL BLOOD LEVEL DETECTOR

K-Number: K823712 · 1983-02-07

ApplicantR. Scott Bell
Decision Date1983-02-07
Product CodeDTW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BEL BLOOD LEVEL DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is R. Scott Bell. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K823712. The device is classified under product code DTW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEL BLOOD LEVEL DETECTOR?

BEL BLOOD LEVEL DETECTOR is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is R. Scott Bell. The 510(k) number is K823712.

When did BEL BLOOD LEVEL DETECTOR receive FDA 510(k) clearance?

BEL BLOOD LEVEL DETECTOR received FDA 510(k) clearance on 1983-02-07, under 510(k) number K823712.

Who is the listed applicant for BEL BLOOD LEVEL DETECTOR?

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

What is the FDA product code for BEL BLOOD LEVEL DETECTOR?

The FDA product code for BEL BLOOD LEVEL DETECTOR is DTW.

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

Related Devices (Code: DTW)

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.

K041558STOCKERTIR PURGE CONTROL (APC) SYSTEMStockert Instrumente GmbHK992857LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070Rocky Mountain Research, Inc.K955152STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMERStoeckert InstrumenteK910599CARDIOPULMONARY BYPASS LEVEL SENSING MONITORJtl Medical Corp.K924354STOCKERT CAPS LOW LEVEL DETECT II/BUBBLE MONITORSorin Biomedica, Fiat, USA, Inc.K915337CAPIOX LEVEL ALARMTerumo 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.

↑