510(k) K771447 · DRX Electrode, Electrocardiograph

PREGELLED DISP. EKG MONITORING ELECT-

Applicant	Hayes Products, Inc., Mchenry IL, US
Decision	Substantially Equivalent, Aug 4, 1977
Received	Aug 2, 1977
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K771447

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.