FDA 510(k) Premarket Notification K943349: MAHURKAR DUAL LUMEN CATHETER

Submission Details & Decision

Normalized public record details for 510(k) notification K943349.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K943349

Applicant / Sponsor

Quinton, Inc.

Device Name

MAHURKAR DUAL LUMEN CATHETER

Product Code

FOZ

Decision Date

1995-03-22

Decision / Status

Unknown (SESK)

Advisory Committee

General Hospital (HO)

Clearance Type

Traditional

Third Party Flag

Date Received

1994-07-12

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