510(k) K881334 · HAM Apparatus, Electrosurgical

LIGHT COAGULATOR LC 250

Applicant	Nk-Optik GmbH, Munich D8000, DE
Decision	Substantially Equivalent, Nov 16, 1989
Received	Mar 30, 1988
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K881334

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.