510(k) K925759 · ERA Otoscope

UNI I

Applicant	Rudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE
Decision	Substantially Equivalent, Jul 26, 1993
Received	Nov 13, 1992
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K925759

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.