510(k) Report

FDA applicant

Robert C. Leif, Ph.D.

Mchenry, IL1 decision1979–19790 recalls

FDA records 1 decision for Robert C. Leif, Ph.D. (Mchenry, IL) in 1979: 1 510(k) clearance. All are in product code IFB (Cytocentrifuge). 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, pathology panel, where it files most

How often FDA has decided Robert C. Leif, Ph.D.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Robert C. Leif, Ph.D. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Robert C. Leif, Ph.D. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IFBCytocentrifuge1decision

What has FDA decided for it lately?

  • K792032Leif Centrifugal Cytology BucketRobert C. Leif, Ph.D. · 1979

The one decision as Robert C. Leif, Ph.D. →

Other applicant names beginning “Robert”

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

Robert Bosch Corp. 21Robert I. Chien & Assoc., Inc. 6Robert R. Moore 5Robert W. Bauer & Assoc., Inc. 3Robert A James 2Robert R. Stevens 2Robert Reid, Inc. 2Robert B. Scott Ocularists of Florida, Inc. 2Robert J. Sislian, Inc. 1Robert C. Cameron 1Robert Shaw Controls Co. 1Robert Bosch Healthcare Systems, Inc. 1