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NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K120182
510(k) Type
Traditional
Applicant
NEOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2012
Days to Decision
90 days
Submission Type
Summary

NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K120182
510(k) Type
Traditional
Applicant
NEOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2012
Days to Decision
90 days
Submission Type
Summary