FDA 510(k)

EVENT MARKER & A SECOND PRESSURE TREND OUTPUT

K-Number: K883518 · 1988-09-22

Decision Date1988-09-22

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

EVENT MARKER & A SECOND PRESSURE TREND OUTPUT is the device name listed in this FDA 510(k) record. The listed applicant is Metatech Corp.. It received FDA 510(k) clearance on 1988-09-22 under 510(k) number K883518. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVENT MARKER & A SECOND PRESSURE TREND OUTPUT?

EVENT MARKER & A SECOND PRESSURE TREND OUTPUT is a medical device that received FDA 510(k) clearance on 1988-09-22. The listed applicant is Metatech Corp.. The 510(k) number is K883518.

When did EVENT MARKER & A SECOND PRESSURE TREND OUTPUT receive FDA 510(k) clearance?

EVENT MARKER & A SECOND PRESSURE TREND OUTPUT received FDA 510(k) clearance on 1988-09-22, under 510(k) number K883518.

Who is the listed applicant for EVENT MARKER & A SECOND PRESSURE TREND OUTPUT?

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

What is the FDA product code for EVENT MARKER & A SECOND PRESSURE TREND OUTPUT?

The FDA product code for EVENT MARKER & A SECOND PRESSURE TREND OUTPUT is GWM.

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Official Source

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