SECHRIST AIRWAY PRESSURE MONITOR MODEL 600— 510(k) K861330

Name: FDA 510(k) clearance K861330
Creator: U.S. Food and Drug Administration
Published: 1986-04-11

Substantially Equivalent

Sechrist Industries, Inc.

FDA 510(k) clearance K861330 for SECHRIST AIRWAY PRESSURE MONITOR MODEL 600, Substantially Equivalent on 1986-04-11. Applicant: Sechrist Industries, Inc.. Device class: 2.

Clearance details

Applicant: Sechrist Industries, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1986-04-09
Decision date: 1986-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

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