NICORE MODEL ESP -1— 510(k) K980937

Name: FDA 510(k) clearance K980937
Creator: U.S. Food and Drug Administration
Published: 2000-09-15

Substantially Equivalent

Nicore Equipment & Leasing, Inc.

FDA 510(k) clearance K980937 for NICORE MODEL ESP -1, Substantially Equivalent on 2000-09-15. Applicant: Nicore Equipment & Leasing, Inc.. Device class: 2.

Clearance details

Applicant: Nicore Equipment & Leasing, Inc.
Product code: Code DRN
Device class: Class 2
Regulation: 21 CFR 870.5225
Advisory panel: Cardiovascular
Date received: 1998-03-12
Decision date: 2000-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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