VENOUS PRESSURE MONITOR, MF 35 LF— 510(k) K790668

Name: FDA 510(k) clearance K790668
Creator: U.S. Food and Drug Administration
Published: 1979-05-23

Substantially Equivalent

Deco Medical, Inc.

FDA 510(k) clearance K790668 for VENOUS PRESSURE MONITOR, MF 35 LF, Substantially Equivalent on 1979-05-23. Applicant: Deco Medical, Inc.. Device class: 2.

Clearance details

Applicant: Deco Medical, Inc.
Product code: Code KRK
Device class: Class 2
Regulation: 21 CFR 870.1140
Advisory panel: Cardiovascular
Date received: 1979-04-06
Decision date: 1979-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K875322 — MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER1988-03-28
K861605 — SCHNEIDER-SHILEY PRESSURE MANOMETER1986-05-28

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