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

SUBCUTANEOUS TISSUE EXPANDER

K Number: K790842 · Decision Aug 3, 1979
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
54
Applicant Total
9
Review Days
93

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Basic Information

Device Name
SUBCUTANEOUS TISSUE EXPANDER
K Number
K790842
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Heyer Schulte Corp.
Date Received
May 2, 1979
Decision Date
August 3, 1979
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

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K760778 T-TUBE DRAIN, ROUND
K760785 MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH
K760784 MISHLER 2 CHAMB FLUSHING VALVE,STAND
K760501 VALVE, STANDARD MODEL PUDENZE FLUSHING