NEOLOOPS— 510(k) K810890

Substantially Equivalent

Medical Marketing Systems

FDA 510(k) clearance K810890 for NEOLOOPS, Substantially Equivalent on 1981-08-31. Applicant: Medical Marketing Systems. Device class: 1.

Clearance details

Applicant: Medical Marketing Systems
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1981-04-02
Decision date: 1981-08-31
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.