Cosmet

FDA 510(k) K933465 · Great Bay Medical Products, Inc.

Substantially Equivalent

510(k) numberK933465

Submission

Device name
Cosmet
Applicant
Great Bay Medical Products, Inc.
Dover, NH, US
Received
July 16, 1993
Decision date
July 20, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KCZ – Prosthesis, Breast, External, Used With Adhesive
Device class
Class I (low risk)
Regulation
21 CFR 878.3800
Specialty
General, Plastic Surgery

Other 510(k)s with product code KCZ

510(k)DeviceApplicantDecision
K990458Straumann Extraoral Implant SystemKCZ · Traditional Straumann USA04/16/1999SE
K951324Maxol Image II Patient Matched Breast ProsthesisKCZ · Traditional Maxol Limited L.C.05/26/1995SE
K932978Calssique or MystiqueKCZ · Traditional Dekumed, Kunststofftechnik Degler GmbH12/22/1993SE
K932899ClassiqueKCZ · Traditional Hemispheres Marketing Co. , Ltd.12/16/1993SE
K933668Almost U, Inc. Breast ProsthesisKCZ · Traditional Almost U., Inc.12/10/1993SE
K921535Suoena Affinity (TM) Model #802KCZ · Traditional Coloplast Corp.05/11/1992SE
K915382Amoena Affinity Model #802KCZ · Traditional Coloplast Corp.01/14/1992SE
K911247Yours Truly Asymmetrical Breast FormKCZ · Traditional Jobst Institute, Inc.03/29/1991SE
K904085Ella Breast FormKCZ · Traditional Coloplast A/S10/31/1990SE
K904316Nouvelle (TM) Model #901, Sizes 0-12, Left & RightKCZ · Traditional Coloplast Corp.10/11/1990SE

Questions and answers

When was Cosmet cleared by the FDA?

Cosmet (K933465) received a 510(k) decision of Substantially Equivalent on July 20, 1994, 369 days after the submission was received.

What is the product code of K933465?

The FDA product code is KCZ – Prosthesis, Breast, External, Used With Adhesive, a Class I (low risk) device regulated under 21 CFR 878.3800.