FDA 510(k), K932184, STERILE LEMAITRE GLOW 'N TELL TAPE

Device Classification Name: Assembly, Thigh/Knee/Shank/Ankle/Foot, External
510(k) Number:    K932184
Device Name:    STERILE LEMAITRE GLOW 'N TELL TAPE
Applicant:     VASCUTECH, INC.
Classification Product Code:    KFX
Date Received:    05/05/1993
Decision Date:    07/22/1993
Decision:    Substantially Equivalent (SESE)
Regulation Medical Specialty:    Physical Medicine
510k Review Panel:    Radiology
Type:    Traditional

43 pages (26 of 69 original pages are fully redacted)