BYZ — Trap, Sterile Specimen Class II

FDA Device Classification

FDA product code BYZ covers "Trap, Sterile Specimen", a Class II medical device regulated under 21 CFR 880.6740. Submissions are reviewed by the General Hospital panel. At least 9 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
BYZ
Device Class
Class II
Regulation Number
880.6740
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K925412ElectromedicsELECTROMEDICS TISSUE TRAP/ #TT280Feb 5, 1993
K913643Medical Device Inspection CoMUCOUS SPECIMEN TRAPOct 10, 1991
K902883Triton TechnologyTISSUE/POLYP TRAP SYSTEMSep 12, 1990
K841409Warne Surgical ProductsBUSH NECK W/PLUGApr 18, 1984
K840253Delta Medical IndustriesONE-WAY AIR VALVEApr 5, 1984
K834467MicrovasiveSPECIMEN TRAPFeb 17, 1984
K822556Bemis Health CareCRITICAL MEASUREMENT UNITOct 18, 1982
K822557Bemis Health CareSPECIMEN ADAPTOROct 18, 1982
K791847Medical Marketing GroupASPRI-LUKEOct 2, 1979