MICRO MPM— 510(k) K940375

Substantially Equivalent

Micro Direct, Inc.

FDA 510(k) clearance K940375 for MICRO MPM, Substantially Equivalent on 1994-11-21. Applicant: Micro Direct, Inc.. Device class: 2.

Clearance details

Applicant: Micro Direct, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1994-01-26
Decision date: 1994-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Auburn, ME, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAP

K201666 — SINGLE USE MANOMETER2020-11-13
K182292 — VORTRAN APM-Plus2019-09-18
K180510 — NS 120P-TRS Airway Pressure Gauge2019-05-01
K172284 — NAPA LP-15 Airway Pressure Monitor2018-02-09
K153733 — VORTRAN Manometer2016-09-16

More clearances from Micro Direct, Inc.

K033688 — MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITY2004-05-19
K031102 — MICROLAB SPIROMETER2003-12-01
K030586 — MICROPEAK2003-08-27
K973314 — SPIROSAFE FILTER1997-11-21
K965042 — MICRODL DIARYCARD SPIROMETER1997-06-17

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