510(k) K932504 · HLJ Ophthalmoscope, Battery-Powered

RI-FORMER

Applicant	Rudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE
Decision	Unknown, Oct 15, 1993
Received	May 21, 1993
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K932504

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.