FDA applicant

Clearview Instruments, Inc.

Stow, MA1 decision1987–19870 recalls

FDA records 1 decision for Clearview Instruments, Inc. (Stow, MA) in 1987: 1 510(k) clearance. All are in product code GKR (System, Hemoglobin, Automated). 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Clearview Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Clearview 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 “Clearview”

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

Clearview Diagnostics, Inc. 2 Clearview Electronics Corp. 1 Clearview Orthopedic Development, LLC 1

Clearview Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Clearview”