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FDA 510(k)

VITELCARE C-TURTLE PATIENT MONITORING SYSTEM

K-Number: K060712 · 2006-04-19

ApplicantVisual Telecommunications Network, Inc.
Decision Date2006-04-19
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITELCARE C-TURTLE PATIENT MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Visual Telecommunications Network, Inc.. It received FDA 510(k) clearance on 2006-04-19 under 510(k) number K060712. 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 VITELCARE C-TURTLE PATIENT MONITORING SYSTEM?

VITELCARE C-TURTLE PATIENT MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is Visual Telecommunications Network, Inc.. The 510(k) number is K060712.

When did VITELCARE C-TURTLE PATIENT MONITORING SYSTEM receive FDA 510(k) clearance?

VITELCARE C-TURTLE PATIENT MONITORING SYSTEM received FDA 510(k) clearance on 2006-04-19, under 510(k) number K060712.

Who is the listed applicant for VITELCARE C-TURTLE PATIENT MONITORING SYSTEM?

The FDA 510(k) record lists Visual Telecommunications Network, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITELCARE C-TURTLE PATIENT MONITORING SYSTEM?

The FDA product code for VITELCARE C-TURTLE PATIENT MONITORING SYSTEM is MWI.

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Other records listing Visual Telecommunications Network, 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.

K043368VITELCARE TURTLE, MODEL 400

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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