FDA applicant

Lynn Peavey Co.

Lenexa, KS1 decision1995–19950 recalls

FDA records 1 decision for Lynn Peavey Co. (Lenexa, KS) in 1995: 1 510(k) clearance. All are in product code JKA (Tubes, Vials, Systems, Serum Separators, Blood…). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Lynn Peavey Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lynn Peavey Co.’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 “Lynn”

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

The Lynn Terrell Co. 1

Lynn Peavey Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lynn”