510(k) Report

FDA applicant

Sscor

Sun Valley, CA5 decisions1994–20041 recall

FDA records 5 decisions for Sscor (Sun Valley, CA) from 1994 to 2004: 5 510(k) clearances. Most are in product codes BTA (Pump, Portable, Aspiration (Manual Or Powered)) and GCX (Apparatus, Suction, Operating-Room, Wall…). Its devices cite 3 predicates, 2 of them its own earlier devices. 1 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 and plastic surgery panel, where it files most

How often FDA has decided Sscor’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sscor since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sscor’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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