MEDI-DYNE APNEA MONITOR— 510(k) K760635

Substantially Equivalent

Med Dyne Inst., Inc.

FDA 510(k) clearance K760635 for MEDI-DYNE APNEA MONITOR, Substantially Equivalent on 1976-09-21. Applicant: Med Dyne Inst., Inc.. Device class: 2.

Clearance details

Applicant: Med Dyne Inst., Inc.
Product code: Code FLS
Device class: Class 2
Regulation: 21 CFR 868.2377
Advisory panel: Anesthesiology
Date received: 1976-09-13
Decision date: 1976-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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