510(k) K001203 · ITX Transducer, Ultrasonic, Diagnostic

OLYMPUS UM 2R/3R ULTRASONIC PROBE AND ASSOCIATED ANCILLARY EQUIPMENT FOR FEMALE REPRODUCTIVE TRACT

Applicant	The Olympus Optical Co., Melville NY, US
Decision	Substantially Equivalent, May 26, 2000
Received	Apr 13, 2000
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K001203

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.