SUCTION SAFETY DEVICE— 510(k) K960937

Substantially Equivalent

R D Intl.

FDA 510(k) clearance K960937 for SUCTION SAFETY DEVICE, Substantially Equivalent on 1996-06-05. Applicant: R D Intl.. Device class: 2.

Clearance details

Applicant: R D Intl.
Product code: Code MJJ
Device class: Class 2
Regulation: 21 CFR 870.4400
Advisory panel: Cardiovascular
Date received: 1996-03-08
Decision date: 1996-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richardson, TX, 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.