FDA 510(k)

MEDACORD PVL, PERSONAL VASCULAR LABORATORY

K-Number: K882018 · 1988-09-21

Decision Date1988-09-21

Product CodeJAF

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MEDACORD PVL, PERSONAL VASCULAR LABORATORY is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1988-09-21 under 510(k) number K882018. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDACORD PVL, PERSONAL VASCULAR LABORATORY?

MEDACORD PVL, PERSONAL VASCULAR LABORATORY is a medical device that received FDA 510(k) clearance on 1988-09-21. The listed applicant is Medasonics, Inc.. The 510(k) number is K882018.

When did MEDACORD PVL, PERSONAL VASCULAR LABORATORY receive FDA 510(k) clearance?

MEDACORD PVL, PERSONAL VASCULAR LABORATORY received FDA 510(k) clearance on 1988-09-21, under 510(k) number K882018.

Who is the listed applicant for MEDACORD PVL, PERSONAL VASCULAR LABORATORY?

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

What is the FDA product code for MEDACORD PVL, PERSONAL VASCULAR LABORATORY?

The FDA product code for MEDACORD PVL, PERSONAL VASCULAR LABORATORY is JAF.

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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.