VACUUM RELIEF VALVE— 510(k) K760894

Substantially Equivalent

Delta Medical Industries

FDA 510(k) clearance K760894 for VACUUM RELIEF VALVE, Substantially Equivalent on 1976-12-09. Applicant: Delta Medical Industries. Device class: 2.

Clearance details

Applicant: Delta Medical Industries
Product code: Code DWD
Device class: Class 2
Regulation: 21 CFR 870.4430
Advisory panel: Cardiovascular
Date received: 1976-10-26
Decision date: 1976-12-09
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.