510(k) K904086

DISCRENE SELF-SUPPORTING BREAST FORM by Coloplast A/S — Product Code KCZ

K904086 is an FDA 510(k) premarket notification submitted by Coloplast A/S for the device "DISCRENE SELF-SUPPORTING BREAST FORM". The FDA issued a decision of Substantially Equivalent on October 2, 1990. The device falls under product code KCZ (Prosthesis, Breast, External, Used With Adhesive), a Class I device regulated under 21 CFR 878.3800. Coloplast A/S has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 2, 1990
Date Received
September 5, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Breast, External, Used With Adhesive
Device Class
Class I
Regulation Number
878.3800
Review Panel
SU
Submission Type