FDA 510(k)

PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC.

K-Number: K896964 · 1990-06-21

Decision Date1990-06-21

Product CodeDSY

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC. is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1990-06-21 under 510(k) number K896964. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC.?

PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC. is a medical device that received FDA 510(k) clearance on 1990-06-21. The listed applicant is Medtronic Vascular. The 510(k) number is K896964.

When did PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC. receive FDA 510(k) clearance?

PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC. received FDA 510(k) clearance on 1990-06-21, under 510(k) number K896964.

Who is the listed applicant for PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC.?

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

What is the FDA product code for PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC.?

The FDA product code for PLASMA TFE VASCULAR PROSTHESIS MODIFIED INSTRUC. is DSY.

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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.