ENGSTOM EDITH— 510(k) K821365

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K821365 for ENGSTOM EDITH, Substantially Equivalent on 1982-06-29. Applicant: Lkb Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code BYD
Device class: Class 1
Regulation: 21 CFR 868.5375
Advisory panel: Anesthesiology
Date received: 1982-05-07
Decision date: 1982-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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