Medical Device Manufacturer · DE , 71004 Boblingen

Hewlett-Packard GmbH - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1995

16

Total

16

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hewlett-Packard GmbH Anesthesiology ✕

3 devices

1-3 of 3

Cleared Sep 11, 1997

HP ORVUE INTRA-OP (M2510A)

Anesthesiology · 262d

Cleared Mar 24, 1995

HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE

Anesthesiology · 11d

Cleared Feb 16, 1995

HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE

Anesthesiology · 245d