510(k) Report

FDA applicant

C.I.S.A. Import Export C/O Larson and Taylor

New York, NY3 decisions1988–19880 recalls

FDA records 3 decisions for C.I.S.A. Import Export C/O Larson and Taylor (New York, NY) in 1988: 3 510(k) clearances. All are in product code HIB (Speculum, Vaginal, Nonmetal). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided C.I.S.A. Import Export C/O Larson and Taylor’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for C.I.S.A. Import Export C/O Larson and Taylor since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — C.I.S.A. Import Export C/O Larson and Taylor 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?

  • HIBSpeculum, Vaginal, Nonmetal3decisions

What has FDA decided for it lately?

  • K880587Autoexpandable Speculum Model Leibovich Medium #3C.I.S.A. Import Export C/O Larson and Taylor · 1988
  • K880586Autoexpandable Speculum Model Leibovich Small #2C.I.S.A. Import Export C/O Larson and Taylor · 1988
  • K880588Autoexpandable Speculum Model Leibovic Large #4C.I.S.A. Import Export C/O Larson and Taylor · 1988

All 3 as C.I.S.A. Import Export C/O Larson and Taylor →