FDA applicant

Kellerandheckman

Washington2 decisions1972–19980 recalls

FDA records 2 decisions for Kellerandheckman (Washington) from 1972 to 1998: 1 510(k) clearance and 1 original PMA approval. All are in product code MED (Sterilant, Medical Devices). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Kellerandheckman since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kellerandheckman

Which product codes does it file in?

What has FDA decided for it lately?