ENGSTROM EMMA ANESTHETIC GAS MONITOR— 510(k) K802614

Name: FDA 510(k) clearance K802614
Creator: U.S. Food and Drug Administration
Published: 1981-01-07

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K802614 for ENGSTROM EMMA ANESTHETIC GAS MONITOR, Substantially Equivalent on 1981-01-07. Applicant: Lkb Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code CBS
Device class: Class 2
Regulation: 21 CFR 868.1620
Advisory panel: Anesthesiology
Date received: 1980-10-21
Decision date: 1981-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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