PM-3— 510(k) K831750

Substantially Equivalent

Delta Medical Industries

FDA 510(k) clearance K831750 for PM-3, Substantially Equivalent on 1983-07-26. Applicant: Delta Medical Industries. Device class: 2.

Clearance details

Applicant: Delta Medical Industries
Product code: Code DXS
Device class: Class 2
Regulation: 21 CFR 870.4310
Advisory panel: Cardiovascular
Date received: 1983-06-01
Decision date: 1983-07-26
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.