FDA 510(k) Premarket Notification K850183: CADD-VT, 5300 AMBULATORY INFUSION PUMP W/3050, 50M

Submission Details & Decision

Normalized public record details for 510(k) notification K850183.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K850183

Applicant / Sponsor

Deltec Systems, Inc.

Device Name

CADD-VT, 5300 AMBULATORY INFUSION PUMP W/3050, 50M

Product Code

FRN

Decision Date

1985-03-13

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

General Hospital (HO)

Clearance Type

Traditional

Third Party Flag

Date Received

1985-01-18

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