MENTOR PATHWAY INTRODUCER/DILATOR— 510(k) K981527

Substantially Equivalent

Mentor Corp.

FDA 510(k) clearance K981527 for MENTOR PATHWAY INTRODUCER/DILATOR, Substantially Equivalent on 1998-07-09. Applicant: Mentor Corp.. Device class: 2.

Clearance details

Applicant: Mentor Corp.
Product code: Code QPB
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 1998-04-28
Decision date: 1998-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Barbara, CA, 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.