TESTCORP ANA— 510(k) K831365

Substantially Equivalent

Catheter Technology Corp.

FDA 510(k) clearance K831365 for TESTCORP ANA, Substantially Equivalent on 1983-06-02. Applicant: Catheter Technology Corp.. Device class: 1.

Clearance details

Applicant: Catheter Technology Corp.
Product code: Code LKS
Device class: Class 1
Regulation: 21 CFR 866.2900
Advisory panel: Microbiology
Date received: 1983-04-26
Decision date: 1983-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K842577 — CATH-TECH POLYURETHANE UMBILICAL VESS1985-03-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.