RMI SOFCLAMP— 510(k) K920676

Substantially Equivalent

Research Medical, Inc.

FDA 510(k) clearance K920676 for RMI SOFCLAMP, Substantially Equivalent on 1992-04-15. Applicant: Research Medical, Inc.. Device class: 2.

Clearance details

Applicant: Research Medical, Inc.
Product code: Code DSS
Device class: Class 2
Regulation: 21 CFR 870.3250
Advisory panel: Cardiovascular
Date received: 1992-02-14
Decision date: 1992-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Midvale, UT, US

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