FDA applicant

Paramed Technology, Inc.

Mountain View, CA3 decisions1979–19890 recalls

FDA records 3 decisions for Paramed Technology, Inc. (Mountain View, CA) from 1979 to 1989: 3 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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 Paramed Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paramed Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Paramed”

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

Paramed S.R.L. 8 Paramed Div 1 Paramed Services, Inc. 1

Paramed Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paramed”