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KMO — Binder, Elastic Class I

FDA Device Classification

Classification Details

Product Code
KMO
Device Class
Class I
Regulation Number
880.5160
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K921852boston pacific medical4 SURE TM RECTAL TUBEOctober 8, 1993
K893809custom hospitals productsCOUGH PILLOWAugust 28, 1989
K883214storer medical productsTHORACIC SUPPORT SYSTEMJanuary 17, 1989
K882592general cardiac technologyHEART HUGGER STERNUM SUPPORT HARNESSSeptember 20, 1988
K792629procter and gamble mfgSTERILIZATION PROCESS/T-BINDERJanuary 11, 1980