ClearanceBrief
510(k) K881010 ยท HET Laparoscope, Gynecologic (And Accessories)

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO

ApplicantSharplan Lasers, Inc., Allendale NJ, US
DecisionSubstantially Equivalent, Apr 21, 1988
ReceivedMar 10, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881010

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.