FDA applicant
Erka Kallmeyer Medizintechnik GmbH
FDA records 1 decision for Erka Kallmeyer Medizintechnik GmbH (Bad Toelz, Bavaria, DE) in 2011: 1 510(k) clearance. All are in product code DXQ (Blood Pressure Cuff). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Erka Kallmeyer Medizintechnik GmbH’s devices, and how often a recall has named them.
FDA decisions per year
1in 2011
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2011.
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