1,2,3 CHANNELL RECORDERS (AR150,AR250,-)— 510(k) K810166

Name: FDA 510(k) clearance K810166
Creator: U.S. Food and Drug Administration
Published: 1981-02-25

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K810166 for 1,2,3 CHANNELL RECORDERS (AR150,AR250,-), Substantially Equivalent on 1981-02-25. Applicant: Honeywell, Inc.. Device class: 1.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1981-01-22
Decision date: 1981-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DSF

view all

K910871 — EDENTEC DIGITAL CHARTER MODEL 37101991-08-29
K912929 — DASH IV1991-08-13
K905856 — MODEL 556 MONITOR1991-01-11
K902586 — GRI LASERGRAPH(TM) ECG PAPER1990-06-22
K902230 — COLORADO COLOR IMAGING RECORDER1990-06-19

More clearances from Honeywell, Inc.

view all

K863100 — CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR1987-02-03
K853501 — HONEYWELL ELECTRONIC VENTILATOR EV-A1986-04-04
K855125 — PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM1986-03-26
K851888 — APM DISPOS. BLOOD PRESSURE TRANSDUCER1985-08-06
K851496 — ECG MONITOR MODEL RM1021985-07-24

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