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FDA 510(k)

VITALMAX 840 SERIES

K-Number: K914164 · 1993-04-09

ApplicantPace Tech Medical Monitors, Inc.
Decision Date1993-04-09
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITALMAX 840 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Pace Tech Medical Monitors, Inc.. It received FDA 510(k) clearance on 1993-04-09 under 510(k) number K914164. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALMAX 840 SERIES?

VITALMAX 840 SERIES is a medical device that received FDA 510(k) clearance on 1993-04-09. The listed applicant is Pace Tech Medical Monitors, Inc.. The 510(k) number is K914164.

When did VITALMAX 840 SERIES receive FDA 510(k) clearance?

VITALMAX 840 SERIES received FDA 510(k) clearance on 1993-04-09, under 510(k) number K914164.

Who is the listed applicant for VITALMAX 840 SERIES?

The FDA 510(k) record lists Pace Tech Medical Monitors, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITALMAX 840 SERIES?

The FDA product code for VITALMAX 840 SERIES is BXN.

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 Pace Tech Medical Monitors, 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.

K970445VITALMAX 4000 CONFIGURED/VITALMAX 4000 MODULAR/VITALMAX 4100/MINIPACK 3100/3000/VITALMAX 800+/MINIPACK 300K932203VITALMAX 530

Related Devices (Code: BXN)

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.

K213049STIMPOD NMS450 Nerve StimulatorXavant Technology (Pty), Ltd.K162086MultiStim ECOPAJUNK GmbH MedizintechnologieK153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorEasy Med Instrument Co., Ltd.K121743EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTINSunmed, LLCK111985MYOGUIDE SYSTEM MODEL 8008Intronix Technologies Corp.K110118STIMTRODE SINGLE USE NERVE STIMULATORXavant Technology (Pty), Ltd.

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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