FDA applicant

Princeton Medical Instruments, Inc.

Mchenry, IL2 decisions1979–19800 recalls

FDA records 2 decisions for Princeton Medical Instruments, Inc. (Mchenry, IL) from 1979 to 1980: 2 510(k) clearances. All are in product code FRN (Pump, Infusion). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Princeton Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Princeton Medical Instruments, 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 “Princeton”

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

Princeton BioMeditech Corp. 72 Princeton Biomedix 14 Princeton Regulatory Assoc. 4 Princeton Applied Research Corp. 2 Princeton Electronic Systems, Inc. 1

Princeton Medical Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Princeton”