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ALPHAMED GEMINI SENSOR, SNORING SENSOR

Page Type
Cleared 510(K)
510(k) Number
K990321
510(k) Type
Traditional
Applicant
ALPHAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1999
Days to Decision
120 days
Submission Type
Summary

ALPHAMED GEMINI SENSOR, SNORING SENSOR

Page Type
Cleared 510(K)
510(k) Number
K990321
510(k) Type
Traditional
Applicant
ALPHAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1999
Days to Decision
120 days
Submission Type
Summary