FDA applicant

Interscience, Inc.

Walker, MI4 decisions1982–19820 recalls

FDA records 4 decisions for Interscience, Inc. (Walker, MI) in 1982: 4 510(k) clearances. Most are in product codes KRZ (Calibrator For Hemoglobin And Hematocrit…) and PPM (General Purpose Reagent). 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 Interscience, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Interscience, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Interscience, 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 “Interscience”

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

Interscience Diagnostics, Inc. 4

Interscience, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Interscience”