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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

LAP DISC 120 X 120, MODEL LD111, LAP DISC 120 X 100, MODEL LD112, LAP DISC 70 X 70, MODEL LD113

Manufacturer

ETHICON ENDO-SURGERY, INC.

Date Cleared

2001-06-18

(87 days)

Product Code

Regulation Number

Type

Panel

General & Plastic Surgery

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K020307,K030824,K070198

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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