FDA applicant

Microwave Medical Systems, Inc.

Littleton, MA5 decisions1990–19990 recalls

FDA records 5 decisions for Microwave Medical Systems, Inc. (Littleton, MA) from 1990 to 1999: 5 510(k) clearances. Most are in product codes KDJ (Set, Administration, For Peritoneal Dialysis…) and DRQ (Amplifier And Signal Conditioner, Transducer…). 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, cardiovascular panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Microwave 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.

See the 510(k) Report

Other applicant names beginning “Microwave”

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

Microwave Development, Inc. 1 Microwave Medical, Inc. 1

Microwave Medical Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Microwave”