510(k) K930576 · HCC Device, Biofeedback

AT42

Applicant	Autoject Systems, Inc., Oak Dale IL, US
Decision	Substantially Equivalent, May 18, 1995
Received	Feb 4, 1993
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K930576

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.