SCANMATE III— 510(k) K921878

Substantially Equivalent

Circadian, Inc.

FDA 510(k) clearance K921878 for SCANMATE III, Substantially Equivalent on 1992-09-11. Applicant: Circadian, Inc.. Device class: 1.

Clearance details

Applicant: Circadian, Inc.
Product code: Code IYP
Device class: Class 1
Regulation: 21 CFR 892.1370
Advisory panel: Radiology
Date received: 1992-04-20
Decision date: 1992-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IYP

K844189 — LINEAR SCANNER PROBE ELSCINT LTD. TL-351985-02-25
K812893 — SUPERFLAB1981-12-08

More clearances from Circadian, Inc.

K894956 — CIRCAMED HOLTER VERSION 41990-02-05
K874641 — CIRCADIAN STRESS TEST II1988-04-01
K874155 — CIRCAMED MONITOR REMOTE START CONDUCTANCE METER1987-11-23
K871251 — CIRCAMED FULL DISCLOSURE SYSTEM1987-05-22
K860973 — CIRCADIAN STRESS TEST SYSTEM1986-08-25

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