Huntleigh Healthcare, Inc.
Huntleigh Healthcare, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2004.
Top product codes for Huntleigh Healthcare, Inc.
Recent clearances by Huntleigh Healthcare, Inc.
- K032315 — IOP8 INTRA OPERATIVE PROBE
- K022786 — DVT60
- K010744 — FLOWTRON UNIVERSAL, MODEL AC600
- K012008 — STS RANGE , MODELS STS20,STS30,STS40
- K002186 — VASCULAR ASSIST
- K010889 — BABY DOPPLEX 3000 MK 2 (BD3000)
- K010894 — BABY DOPPLEX 3002 (BD3002)
- K001882 — BABY DOPPLEX 4002-TWINS, MODEL BD4002
- K990569 — BABY DOPPLEX 4000, MODEL BD 4000
- K984307 — MODIFICATION OF: RHEO DOPPLEX II
- K965153 — HUNTLEIGH FP5000 SYSTEM MODEL FP5000
- K963711 — BABY DOPPLEX (3000)
- K930200 — MULTI DOPPLEX II / FETAL DOPPLEX II
- K925717 — CALF GARMENT DVT10(S) COMPRESSIBLE LIMB SLEEVE
Data sourced from openFDA. This site is unofficial and independent of the FDA.