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FDA 510(k)

MEDVISION PERSONAL MONITOR

K-Number: K961343 · 1997-03-13

ApplicantMedvision, Inc.
Decision Date1997-03-13
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDVISION PERSONAL MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Medvision, Inc.. It received FDA 510(k) clearance on 1997-03-13 under 510(k) number K961343. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDVISION PERSONAL MONITOR?

MEDVISION PERSONAL MONITOR is a medical device that received FDA 510(k) clearance on 1997-03-13. The listed applicant is Medvision, Inc.. The 510(k) number is K961343.

When did MEDVISION PERSONAL MONITOR receive FDA 510(k) clearance?

MEDVISION PERSONAL MONITOR received FDA 510(k) clearance on 1997-03-13, under 510(k) number K961343.

Who is the listed applicant for MEDVISION PERSONAL MONITOR?

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

What is the FDA product code for MEDVISION PERSONAL MONITOR?

The FDA product code for MEDVISION PERSONAL MONITOR is GCJ.

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Related Devices (Code: GCJ)

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Official Source

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