FLEXLAB 3.6, ACCELERATOR A3600— 510(k) K121012

Substantially Equivalent

Inpeco S.P.A.

FDA 510(k) clearance K121012 for FLEXLAB 3.6, ACCELERATOR A3600, Substantially Equivalent on 2012-08-31. Applicant: Inpeco S.P.A.. Device class: 2.

Clearance details

Applicant
Inpeco S.P.A.
Product code
Code CEM
Device class
Class 2
Regulation
21 CFR 862.1600
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Segrate, Milan, IT
Download summary PDFView on FDA.gov ↗

Recent devices under product code CEM

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Recalls naming K121012

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K121012.

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