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FDA 510(k)

VITAL SIGNS MONITOR, PROPAQ LT

K-Number: K033378 · 2004-03-01

ApplicantWelch Allyn Protocol, Inc.
Decision Date2004-03-01
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITAL SIGNS MONITOR, PROPAQ LT is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn Protocol, Inc.. It received FDA 510(k) clearance on 2004-03-01 under 510(k) number K033378. 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 VITAL SIGNS MONITOR, PROPAQ LT?

VITAL SIGNS MONITOR, PROPAQ LT is a medical device that received FDA 510(k) clearance on 2004-03-01. The listed applicant is Welch Allyn Protocol, Inc.. The 510(k) number is K033378.

When did VITAL SIGNS MONITOR, PROPAQ LT receive FDA 510(k) clearance?

VITAL SIGNS MONITOR, PROPAQ LT received FDA 510(k) clearance on 2004-03-01, under 510(k) number K033378.

Who is the listed applicant for VITAL SIGNS MONITOR, PROPAQ LT?

The FDA 510(k) record lists Welch Allyn Protocol, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAL SIGNS MONITOR, PROPAQ LT?

The FDA product code for VITAL SIGNS MONITOR, PROPAQ LT is MWI.

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Other records listing Welch Allyn Protocol, 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.

K070204LINK TO ACUITY CLINICIAN NOTIFIERK063419MODIFICATION TO VSM- VITAL SIGNS MONITOR, (VSM 300 )K031740VSM - VITAL SIGNS MONITOR, MODEL 53000 SERIESK022453MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEMK021681MICROPAQ, MODELS 402, 404K012451PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246

View all 7 devices →

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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