PERITONEAL INTRODUCER & SHEATH— 510(k) K771529

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K771529 for PERITONEAL INTRODUCER & SHEATH, Substantially Equivalent on 1977-08-16. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code GYK
Advisory panel: Neurology
Date received: 1977-08-08
Decision date: 1977-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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