Medical Device Manufacturer · US , Doylestown , PA

Neoforce Group, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

Recent clearances: PRESSURE MANOMETER, NEOPIP PATIENT CIRCUIT WITH PEEP, NEOPOP INFANT RESUSCITATOR WITH FLOW METER

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Neoforce Group, Inc. Anesthesiology ✕

6 devices

1-6 of 6

Cleared Jun 10, 2011

PRESSURE MANOMETER

Anesthesiology · 143d

Cleared Apr 20, 2011

NEOPIP PATIENT CIRCUIT WITH PEEP

Anesthesiology · 111d

Cleared Jan 06, 2011

NEOPOP INFANT RESUSCITATOR WITH FLOW METER

Anesthesiology · 114d

Cleared Oct 07, 2009

ISPIRA RESUSCITATION UNIT

Anesthesiology · 90d

Cleared Sep 12, 2007

NEOPIP INFANT RESUSCITATOR

Anesthesiology · 51d

Cleared May 29, 2007

NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP

Anesthesiology · 106d