OHMEDA MODEL 0001/0003 RECORDER— 510(k) K851274

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K851274 for OHMEDA MODEL 0001/0003 RECORDER, Substantially Equivalent on 1985-05-15. Applicant: Ohmeda Medical. Device class: 1.

Clearance details

Applicant: Ohmeda Medical
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1985-04-01
Decision date: 1985-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, 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.