SECHRIST AIRWAY PRESSURE MONITOR #400— 510(k) K810648

Name: FDA 510(k) clearance K810648
Creator: U.S. Food and Drug Administration
Published: 1981-03-20

Substantially Equivalent

Sechrist Industries, Inc.

FDA 510(k) clearance K810648 for SECHRIST AIRWAY PRESSURE MONITOR #400, Substantially Equivalent on 1981-03-20. 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: 1981-03-11
Decision date: 1981-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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