Medical Device Manufacturer · US , Washington , DC

Heyer America, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1991

Recent clearances: MODULAR, NARKOMAT, MODEL 2000, ANODYNE CC

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Heyer America, Inc. Anesthesiology ✕

4 devices

1-4 of 4

Cleared Feb 05, 2001

Anesthesiology · 221d

Cleared Oct 11, 2000

NARKOMAT, MODEL 2000

Anesthesiology · 197d

Cleared Aug 11, 1997

Anesthesiology · 342d

Cleared Aug 20, 1991

MINITROP AEROSOL UNIT

Anesthesiology · 70d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Sep 13, 2026