Calgon Vestal Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Calgon Vestal Div. - FDA 510(k) Cleared Devices
19
Total
17
Cleared
0
Denied
Calgon Vestal Div. has 17 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 17 cleared submissions from 1989 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Calgon Vestal Div. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Calgon Vestal Div.
19 devices
Cleared
Oct 19, 1994
ALSA-KLENZ
General Hospital
36d
Cleared
Oct 07, 1994
BILL EVANS-KLENZ
General Hospital
51d
Cleared
Aug 04, 1994
SAF-GEL HYDRATING DERMAL WOUND DRESSING
General & Plastic Surgery
86d
Cleared
Jun 17, 1994
AMERSE
General Hospital
450d
Cleared
May 26, 1994
LPH
General Hospital
435d
Cleared
May 26, 1994
VESTA-SYDE(R) INTERIM INSTR DECONTAMINATION SYSTEM
General Hospital
413d
Cleared
May 18, 1994
MON-KLENZ
General Hospital
68d
Cleared
May 16, 1994
VESPHENE II
General Hospital
412d
Cleared
May 12, 1994
LONZA FORMULATION R-82
General Hospital
365d
Cleared
Jul 08, 1993
HYDRASORB STERILE DRESSING
General & Plastic Surgery
98d
Cleared
Apr 20, 1993
EPI-LOCK WOUND DRESSING
General & Plastic Surgery
140d
Cleared
May 29, 1992
KALTOSTAT FORTEX WOUND DRESSING
General & Plastic Surgery
87d
Cleared
Oct 23, 1991
FORTEX(TM) WOUND DRESSING
General & Plastic Surgery
27d
Cleared
Mar 20, 1991
KALTOSTAT WOUND DRESSING
General & Plastic Surgery
70d
Cleared
Mar 20, 1991
KALTOSTAT WOUND PACKING
General & Plastic Surgery
70d
Cleared
Dec 12, 1990
KALTOSTAT WOUND DRESSING
General & Plastic Surgery
71d
Cleared
Aug 23, 1989
KALTOCARB WOUND DRESSING
General & Plastic Surgery
40d
Cleared
Jul 14, 1989
KALTOSTAT WOUND PACKING
General & Plastic Surgery
86d
Cleared
Jun 23, 1989
KALTOSTAT(TM) WOUND DRESSING
General & Plastic Surgery
78d