510(k) Report

FDA applicant

Creative Laboratory Products, Inc.

Indianapolis, IN27 decisions1988–19950 recalls

FDA records 27 decisions for Creative Laboratory Products, Inc. (Indianapolis, IN) from 1988 to 1995: 27 510(k) clearances. Most are in product codes JJY (Multi-Analyte Controls, All Kinds (Assayed)) and JJX (Single (Specified) Analyte Controls (Assayed…). 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, clinical chemistry panel, where it files most

How often FDA has decided Creative Laboratory Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Creative Laboratory Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Creative Laboratory Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Creative”

FDA records each applicant name separately; these may or may not be the same firm.