Medical Device Manufacturer · US , Guntersville , AL

Kappler, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kappler, Inc. General Hospital ✕

2 devices

1-2 of 2

Cleared Mar 29, 1994

KAPPLER PRO/VENT PROCEDURE GOWN

General Hospital · 299d

Cleared Mar 29, 1994

KAPPLER PRO/VENT BOOT

General Hospital · 295d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Apr 28, 2026