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FDA 510(k)

MVL/MODULAB WITH PVR MODULE

K-Number: K884624 · 1989-02-01

ApplicantLife Sciences Manufacturing, Inc.
Decision Date1989-02-01
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MVL/MODULAB WITH PVR MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Life Sciences Manufacturing, Inc.. It received FDA 510(k) clearance on 1989-02-01 under 510(k) number K884624. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVL/MODULAB WITH PVR MODULE?

MVL/MODULAB WITH PVR MODULE is a medical device that received FDA 510(k) clearance on 1989-02-01. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K884624.

When did MVL/MODULAB WITH PVR MODULE receive FDA 510(k) clearance?

MVL/MODULAB WITH PVR MODULE received FDA 510(k) clearance on 1989-02-01, under 510(k) number K884624.

Who is the listed applicant for MVL/MODULAB WITH PVR MODULE?

The FDA 510(k) record lists Life Sciences Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MVL/MODULAB WITH PVR MODULE?

The FDA product code for MVL/MODULAB WITH PVR MODULE is JOM.

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Other records listing Life Sciences Manufacturing, 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.

K910905SFA-II MICROPROCESSOR-CONTROLLED MODULEK903700IPG-II MODULEK900365PAG MICROPROCESSOR-CONTROLLED MODULEK896500CWD/PPG MODULEK895588PORTABLE AIR PLETHYSMOGRAPHK896528SFA MODULE

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Related Devices (Code: JOM)

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K220527PADnet XpressCollaborative Care Diagnostics, LLC, D.B.A. BiomedixK213730MESI mTABLET TBI diagnostic system, MESI mTABLET TBIMesi, Development of Medical Devices, Ltd.; Mesi D.O.O.K200567ASI Plethysmogrpah AnalyzerArterial Stiffness, Inc.K201046Automated ankle brachial pressure index measuring device, MESI mTABLET systemMesi D.O.O.; Mesi, Development of Medical Devices, Ltd.K191266VitalScan ANSMedeia, Inc.K172655Automated ankle brachial pressure index measuring deviceMesi D.O.O.; Mesi, Development of Medical Devices, 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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