Medical Device Manufacturer · US , Ontario , CA

The Kipp Group - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1997

Recent clearances: KIPP MED I.V. MANIFOLD

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - The Kipp Group General Hospital ✕

6 devices

1-6 of 6

Cleared Mar 01, 2000

General Hospital · 27d

Cleared Feb 29, 2000

KIPPMED I.V. MANIFOLD

General Hospital · 41d

Cleared Nov 02, 1999

General Hospital · 42d

Cleared Sep 15, 1999

NAC PRN NEEDLELESS ACCESS CONNECTOR

General Hospital · 71d

Cleared Aug 20, 1999

INTRAVASCULAR ADMINISTRATION SET

General Hospital · 73d

Cleared Apr 14, 1997

KIPP MED I.V. MANIFOLD

General Hospital · 82d