Radovan Tissue Expander

FDA 510(k) K842883 · Mentor Corp.

Substantially Equivalent

510(k) numberK842883

Submission

Device name
Radovan Tissue Expander
Applicant
Mentor Corp.
Mchenry, IL, US
Received
July 23, 1984
Decision date
August 17, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LCJ – Tissue Expander And Accessories
Device class
Unclassified
Implant
Yes

Other 510(k)s with product code LCJ

510(k)DeviceApplicantDecision
K254126Natrelle 133S Tissue ExpandersLCJ · Special AbbVie01/16/2026SE
K242963MENTOR™ PliaForm™ Breast Tissue Expander w/ Suture TabsLCJ · Traditional Mentor Worldwide, LLC04/24/2025SE
K243836Mentor™ CPX ™ 4 PLUS Enhance Breast Tissue ExpanderLCJ · Special Mentor Worldwide, LLC01/12/2025SE
K241918MENTOR™ CPX™4 PLUS Enhance Breast Tissue ExpanderLCJ · Special Mentor Worldwide, LLC08/02/2024SE
K211676Motiva Flora SmoothSilk Tissue ExpanderLCJ · Traditional Motiva USA, LLC10/13/2023SE
K214124AlloX2 Pro Tissue ExpandersLCJ · Traditional Sientra, Inc.06/08/2023SE
K221127Sientra, inc. PortfinderLCJ · Traditional Sientra, Inc.05/10/2023SE
K180826Natrelle 133 Plus MICROCELL Tissue ExpanderLCJ · Traditional Allergan12/21/2018SE
K182335CPX 4 Breast Tissue Expander with Smooth SurfaceLCJ · Special Mentor Worldwide, LLC09/25/2018SE
K182054Natrelle 133S Tissue ExpanderLCJ · Special Allergan08/29/2018SE

More from Allergan

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K050148Mentor Aris Trans-Obturator Tape and Surgical KitOTN · Traditional 03/09/2005SE
K042851Mentor Obtape Trans-Obturator Surgical KitOTN · Special 11/09/2004SE
K040959Mentor Genesis Penile ProsthesisFAE · Traditional 10/29/2004SE
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Questions and answers

When was Radovan Tissue Expander cleared by the FDA?

Radovan Tissue Expander (K842883) received a 510(k) decision of Substantially Equivalent on August 17, 1984, 25 days after the submission was received.

What is the product code of K842883?

The FDA product code is LCJ – Tissue Expander And Accessories, a Unclassified device.