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FDA PRODUCT CODE · CLASS II

PSYWhole Slide Imaging System

The whole slide imaging system is an automated digital slide creation, viewing, and management system intended as an aid to the pathologist to review and interpret digital images of surgical pathology slides prepared from formalin-fixed, paraffin-embedded (FFPE) tissue. The system generates digital images that would otherwise be appropriate for manual visualization by conventional brightfield microscopy. The whole slide imaging system is not intended for use with slides prepared from frozen tissue, cytology, and non-FFPE hematopathology specimens (e.g., peripheral blood smear).

DEVICE CLASS
Class II
REGULATION
21 CFR 864.3700
MEDICAL SPECIALTY
Pathology
REVIEW PANEL
PA
ImplantLife-sustainingGMP-exemptThird-party review eligible
7
510(K)/PMA CLEARANCES
510k: 7
0
RECALL ENTRIES

Recent clearances

K251952Virasoft Corporation · 510k2026-07-17
K253606Hamamatsu Photonics K.K. · 510k2026-07-15
K243871Philips Medical Systems Nederland B.V. · 510k2025-03-06
K241717Shandon Diagnostics Limited · 510k2025-02-28
K242783Ventana Medical Systems, Inc. · 510k2024-12-17
K242848Philips Medical Systems Nederland B.V. · 510k2024-12-10
K241871Philips Medical Systems Nederland B.V. · 510k2024-12-02

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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