510(k) Report

FDA applicant

Microtech Medical Systems, Inc.

Aurora, CO13 decisions1977–19950 recalls

FDA records 13 decisions for Microtech Medical Systems, Inc. (Aurora, CO) from 1977 to 1995: 12 510(k) clearances and 1 original PMA approval. Most are in product codes JWY (Manual Antimicrobial Susceptibility Test Systems) and JTC (Device, Microtiter Diluting/Dispensing). 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, microbiology panel, where it files most

How often FDA has decided Microtech Medical Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microtech Medical Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Microtech Medical Systems, 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 “Microtech”

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