FDA applicant

Select Sources, Inc.

Los Angeles, CA7 decisions1986–19890 recalls

FDA records 7 decisions for Select Sources, Inc. (Los Angeles, CA) from 1986 to 1989: 7 510(k) clearances. Most are in product codes HIS (Condom) and FMF (Syringe, Piston). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Select Sources, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Select”

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

Select Medical Systems, Inc. 6 Select Medizintechnik Hermann Sutter GmbH 1 Select Fabricators, Inc. 1 Select Labs, LLC 1

Select Sources, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Select”