Resmed, Ltd.

Resmed, Ltd. holds 103 FDA 510(k) medical device clearances, first cleared 1996, most recent 2019, with 11 FDA device recalls on record.

Clearances by Resmed, Ltd. — page 2

101–103 of 103

K970771 — SULLIVAN AUTOSET PORTABLE II NASAL CPAP SYSTEMCode BZD·1997-06-20
K970516 — SULLIVAN AUTOSET HOME NASAL CPAP SYSTEMCode BZD·1997-05-09
K961783 — SULLIVAN VPAP II ST NASAL VPAP SYSTEMCode BZD·1996-08-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.