510(k) Report

FDA applicant

In Vitro Scientific Products

Oak View, CA1 decision1987–19870 recalls

FDA records 1 decision for In Vitro Scientific Products (Oak View, CA) in 1987: 1 510(k) clearance. All are in product code KJC (Bottle, Roller, Tissue Culture). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, hematology panel, where it files most

How often FDA has decided In Vitro Scientific Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for In Vitro Scientific Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — In Vitro Scientific Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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