Huntleigh Technology, Inc.
Huntleigh Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1999.
Top product codes for Huntleigh Technology, Inc.
Recent clearances by Huntleigh Technology, Inc.
- K992733 — AKRON ATP9 TRACTION MACHINE
- K964699 — RHEO DOPPLEX II (RD 2)
- K924516 — OP3/VP4
- K910188 — FLOWPLUS AC330 PUMP GARMENTS
- K900882 — MULTI DOPPLEX, MD-1
- K900618 — HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140
- K890012 — HUNTLEIGH DYNAMIC FLOTATION SYSTEM
- K884451 — DOPCORD PPG
- K881632 — FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT
- K874688 — FLOWTRON AC200/2
- K882644 — HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5
- K871271 — HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR.
- K871272 — HUNTLEIGH FLOWPAC FP2000
- K870681 — HUNTLEIGH BETA II HM85
- K854267 — HUNTLEIGH DOPCORD, D140
- K850910 — HUNTLEIGH FLOWTRON AIR, AC400/2 AIR
- K850945 — HUNTLEIGH FLOWTRON AIR HAND GARMENT, HG300
- K844879 — HUNTLEIGH ALPHACARE, HM95 ALTERNATING PRESS-PUMP
- K844880 — HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES
- K834399 — NEW MOTHER'S WAY-BREAST PUMP
- K823081 — M2100 ANTEPARTUM FETAL MONITOR
- K823188 — M2000 INTRAPARTUM FETAL MONITOR
- K810115 — DOPPLEX-PLB & PXB
Data sourced from openFDA. This site is unofficial and independent of the FDA.