AIM-V (R) MEDIUM, MODEL 087-0112— 510(k) K022086

Name: FDA 510(k) clearance K022086
Creator: U.S. Food and Drug Administration
Published: 2002-12-23

Substantially Equivalent

Invitrogen Corporation

FDA 510(k) clearance K022086 for AIM-V (R) MEDIUM, MODEL 087-0112, Substantially Equivalent on 2002-12-23. Applicant: Invitrogen Corporation. Device class: 2.

Clearance details

Applicant: Invitrogen Corporation
Product code: Code NDS
Device class: Class 2
Regulation: 21 CFR 876.5885
Advisory panel: Gastroenterology, Urology
Date received: 2002-06-27
Decision date: 2002-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Island, NY, US

Download summary PDF View on FDA.gov ↗

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Recalls naming K022086

K-number listed on FDA's recall record

Z-2543-2018 — GIBCO CTS AIM V Serum-Free Media (SFM), Model Number 0870112BK. Tissue and cell culture medium.Class II·Terminated·Life Technologies, Corp.·20180510

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K022086.

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