EC6 PLETHYSMOGRAPH— 510(k) K982707

Substantially Equivalent

D. E. Hokanson, Inc.

FDA 510(k) clearance K982707 for EC6 PLETHYSMOGRAPH, Substantially Equivalent on 1998-08-26. Applicant: D. E. Hokanson, Inc.. Device class: 2.

Clearance details

Applicant: D. E. Hokanson, Inc.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1998-08-03
Decision date: 1998-08-26
Decision: Substantially Equivalent
Clearance type: Special
Location: Bellevue, WA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOM

K220527 — PADnet Xpress2022-10-20
K213730 — MESI mTABLET TBI diagnostic system, MESI mTABLET TBI2022-04-21
K200567 — ASI Plethysmogrpah Analyzer2021-02-26
K201046 — Automated ankle brachial pressure index measuring device, MESI mTABLET system2020-12-11
K191266 — VitalScan ANS2020-01-15

More clearances from D. E. Hokanson, Inc.

K041689 — POLYURETHANE BLOOD PRESSURE CUFFS2004-08-06
K033156 — OB1 OBSTETRICAL DOPPLER2003-12-09
K023707 — A16 BLOOD FLOW MEASUREMENT SYSTEM2003-02-12
K973426 — ANS 2000 ECG MONITOR AND RESPIRATION PACER1998-08-12
K970570 — NIVP3 (WINDOWS VERSION OF NIVP1997-10-03

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