Medical Device Manufacturer · US , St. Louis , MO

Calgon Vestal Div. - FDA 510(k) Cleared Devices

19 submissions · 17 cleared · Since 1989

19

Total

17

Cleared

0

Denied

FDA 510(k) Regulatory Record - Calgon Vestal Div. General Hospital ✕

8 devices

1-8 of 8

Cleared Oct 19, 1994

General Hospital · 36d

Cleared Oct 07, 1994

BILL EVANS-KLENZ

General Hospital · 51d

Cleared Jun 17, 1994

General Hospital · 450d

Cleared May 26, 1994

General Hospital · 435d

Cleared May 26, 1994

VESTA-SYDE(R) INTERIM INSTR DECONTAMINATION SYSTEM

General Hospital · 413d

Cleared May 18, 1994

General Hospital · 68d

Cleared May 16, 1994

General Hospital · 412d

Cleared May 12, 1994

LONZA FORMULATION R-82

General Hospital · 365d