510(k) Report

FDA applicant

Creative Scientific Equipment Corp.

Long Beach, CA1 decision1988–19880 recalls

FDA records 1 decision for Creative Scientific Equipment Corp. (Long Beach, CA) in 1988: 1 510(k) clearance. All are in product code SCL (Allergen And Vaccine Delivery Needles). 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, general hospital panel, where it files most

How often FDA has decided Creative Scientific Equipment Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Creative Scientific Equipment Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Creative Scientific Equipment Corp.’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.