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