FDA applicant

Santa Barbara Medco, Inc.

Mchenry, IL8 decisions1980–19850 recalls

FDA records 8 decisions for Santa Barbara Medco, Inc. (Mchenry, IL) from 1980 to 1985: 8 510(k) clearances. Most are in product codes FTY (Tape, Measuring, Rulers And Calipers) and ETD (Tube, Tympanostomy). 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 and plastic surgery panel, where it files most

How often FDA has decided Santa Barbara Medco, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Santa Barbara Medco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Santa Barbara Medco, 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 “Santa”

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

Santa Barbara Imaging Systems 2 Santa FE Swim Systems 1

Santa Barbara Medco, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Santa”