PEAKLOG AND DISPLAY SOFTWARE— 510(k) K940835

Name: FDA 510(k) clearance K940835
Creator: U.S. Food and Drug Administration
Published: 1994-11-01

Substantially Equivalent

Medtrac Technologies Corp.

FDA 510(k) clearance K940835 for PEAKLOG AND DISPLAY SOFTWARE, Substantially Equivalent on 1994-11-01. Applicant: Medtrac Technologies Corp.. Device class: 2.

Clearance details

Applicant: Medtrac Technologies Corp.
Product code: Code BZH
Device class: Class 2
Regulation: 21 CFR 868.1860
Advisory panel: Anesthesiology
Date received: 1994-02-23
Decision date: 1994-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakewood, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZH

view all

K253180 — Microlife Digital Peak Flow Meter, Model PF200B (PF200B)2026-06-23
K252802 — Peak Flow Meter (PF-10(BR-PEF231))2026-05-29
K241338 — Peak Flow Meter2024-12-31
K232588 — Aluna 22024-11-25
K230423 — Electronic Peak Flow Meter2024-02-23

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