FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER

K Number: K865056 · Decision May 22, 1987
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
54
Applicant Total
11
Review Days
149

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Basic Information

Device Name
CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER
K Number
K865056
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Cox-Uphuff Intl.
Date Received
December 24, 1986
Decision Date
May 22, 1987
Product Code
LCJ
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LCJ Tissue Expander And Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LCJ), ordered by most recent decision date.

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Other Clearances by Cox-Uphuff Intl.

K Number Device Name
K874276 CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER
K874342 LIGATURE CARRIER/PACKER, HYDROXYLAPATITE
K873470 TEMPLATE
K871200 CUI NASAL SEPTUM BUTTON
K865033 BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER
K854339 CUI CHIN SIZER
K853945 CUI RHINOPLASTY IMPLANTS
K831566 CUI MAMMARY PROTHESIS SIZER
K813394 DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM
K802214 COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
Search all 11 clearances from Cox-Uphuff Intl. →