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ANTI-SNORING DEVICE OR ASD

Page Type
Cleared 510(K)
510(k) Number
K011723
510(k) Type
Traditional
Applicant
PI MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2002
Days to Decision
562 days
Submission Type
Summary

ANTI-SNORING DEVICE OR ASD

Page Type
Cleared 510(K)
510(k) Number
K011723
510(k) Type
Traditional
Applicant
PI MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2002
Days to Decision
562 days
Submission Type
Summary