RECOMED BLOOD-FLOW METER H236-052-02— 510(k) K840522

Name: FDA 510(k) clearance K840522
Creator: U.S. Food and Drug Administration
Published: 1985-05-16

Substantially Equivalent

Litton Medical Electronics

FDA 510(k) clearance K840522 for RECOMED BLOOD-FLOW METER H236-052-02, Substantially Equivalent on 1985-05-16. Applicant: Litton Medical Electronics. Device class: 2.

Clearance details

Applicant: Litton Medical Electronics
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1984-02-07
Decision date: 1985-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elk Grove Village, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DPW

view all

K260700 — BlueDop Vascular Expert2026-07-08
K252810 — FloPatch FP1202026-04-24
K251904 — VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01) +1 more2025-11-20
K251114 — FloPatch FP1202025-06-20
K243852 — Elfor-L2025-04-14

More clearances from Litton Medical Electronics

view all

K840439 — RECOMED CARDIAC OUTPUT METER 236067-1984-11-20
K840899 — SERVOMED ARRHYCOMP CENTRAL MONITOR SYS1984-11-20
K840523 — SERVOMED PULSE AMPLIFIER MODULE-206-1984-10-29
K840524 — SERVOMED BASIC BEDSIDE UNIT SMV 110TP1984-10-26
K840209 — SERVOMED MEDIVISION SCOPE SMV-2351984-09-20

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