510(k) K952797 · HCC Device, Biofeedback

AT53 DUAL CHANNEL EMG

Applicant	Stoelting Co., Wood Dale IL, US
Decision	Substantially Equivalent, Apr 17, 1996
Received	Jun 19, 1995
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K952797

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.