510(k) K182407 · QAI Powered Microneedle Device

Exceed Microneedling device

Applicant	Mt. Derm GmbH, Berlin, DE
Decision	Substantially Equivalent, Jul 19, 2019
Received	Sep 4, 2018
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K182407

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.