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VEINOPLUS NEUROMUSCULAR STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K072252
510(k) Type
Traditional
Applicant
ADREM TECHNOLOGY SARL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2008
Days to Decision
170 days
Submission Type
Summary

VEINOPLUS NEUROMUSCULAR STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K072252
510(k) Type
Traditional
Applicant
ADREM TECHNOLOGY SARL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2008
Days to Decision
170 days
Submission Type
Summary