NEWMED ABP-LITE— 510(k) K955887

Substantially Equivalent

Newmed Corp.

FDA 510(k) clearance K955887 for NEWMED ABP-LITE, Substantially Equivalent on 1996-09-05. Applicant: Newmed Corp.. Device class: 2.

Clearance details

Applicant: Newmed Corp.
Product code: Code DXW
Device class: Class 2
Regulation: 21 CFR 870.1270
Advisory panel: Cardiovascular
Date received: 1995-12-28
Decision date: 1996-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.