Circadian, Inc.
Circadian, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1992.
Top product codes for Circadian, Inc.
Recent clearances by Circadian, Inc.
- K921878 — SCANMATE III
- K894956 — CIRCAMED HOLTER VERSION 4
- K874641 — CIRCADIAN STRESS TEST II
- K874155 — CIRCAMED MONITOR REMOTE START CONDUCTANCE METER
- K871251 — CIRCAMED FULL DISCLOSURE SYSTEM
- K860973 — CIRCADIAN STRESS TEST SYSTEM
- K851517 — CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO
- K851643 — REMOTE CONTROL MODULE
- K840741 — PULMONARY FUNCTION TESTING STS
- K833619 — CONDUCTANCE METER
- K830830 — CIRCA MED TWO-CHANNEL
- K810698 — PHARMALOG
- K800214 — CIRCAMED I
Data sourced from openFDA. This site is unofficial and independent of the FDA.