Sims Deltec, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sims Deltec, Inc. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
Sims Deltec, Inc. has 32 FDA 510(k) cleared general hospital devices. Based in St. Paul, US.
Historical record: 32 cleared submissions from 1995 to 2001.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sims Deltec, Inc.
32 devices
Cleared
Mar 08, 2001
PROPORT PLASTIC VENOUS IMPLANTABLE ACCESS SYSTEMS PRE-ASSEMBLED WITH SILICONE...
General Hospital
23d
Cleared
Jun 08, 2000
CADD-PRIZM PCS II MODEL 6101 AMBULATORY INFUSION SYSTEM
General Hospital
85d
Cleared
Apr 27, 2000
CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090
General Hospital
35d
Cleared
Jan 27, 2000
PLASTIC PORT IMPLANTABLE VENOUS ACCESS SYSTEM
General Hospital
43d
Cleared
Nov 18, 1999
PORT-A-CATH II TRANS-ARTERIAL PERCUTANEOUS SYSTEM
General Hospital
99d
Cleared
Oct 19, 1999
P.A.S. PORT ELITE IMPLANTABLE VENOUS ACCESS SYSTEM
General Hospital
53d
Cleared
Jun 15, 1999
CADD ADMINISTRATION SET
General Hospital
36d
Cleared
Jun 09, 1999
CADD-TPN ADMINISTRATION SET, MODEL 21-7071
General Hospital
57d
Cleared
Jun 09, 1999
CADD-PRIZM HIGH VOLUME ADMINISTRATION SET WITH 1.2 U FILTER AND ADD-ON...
General Hospital
54d
Cleared
Feb 12, 1999
CADD ADMINISTRATION SET, CADD 250ML FLEXIBLE MEDICATION RESERVOIR, MODIFIED...
General Hospital
32d
Cleared
Jan 29, 1999
CLINICATH POLYFLOW POLYURETHANE PERIPHERALLY INSERTED CATHETERS
General Hospital
77d
Cleared
Nov 04, 1998
CADD-LEGACY 1 AMBULATORY INFUSION SYSTEM MODEL NUMBER 6400
General Hospital
84d