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FDA 510(k)

DATACAPTOR

K-Number: K032142 · 2003-08-08

ApplicantCapsule Technologie
Decision Date2003-08-08
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATACAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Capsule Technologie. It received FDA 510(k) clearance on 2003-08-08 under 510(k) number K032142. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATACAPTOR?

DATACAPTOR is a medical device that received FDA 510(k) clearance on 2003-08-08. The listed applicant is Capsule Technologie. The 510(k) number is K032142.

When did DATACAPTOR receive FDA 510(k) clearance?

DATACAPTOR received FDA 510(k) clearance on 2003-08-08, under 510(k) number K032142.

Who is the listed applicant for DATACAPTOR?

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

What is the FDA product code for DATACAPTOR?

The FDA product code for DATACAPTOR is MWI.

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 Capsule Technologie 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.

K183638SmartLinx Vitals Plus Patient Monitoring SystemK180734SmartLinx Vitals Plus Patient Monitoring SystemK020197MODIFICATION TO DATACAPTORK013019DATACAPTOR

Related Devices (Code: MWI)

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.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

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.

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