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SNORING CONTROL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963591
510(k) Type
Traditional
Applicant
KENNETH HILSEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1998
Days to Decision
487 days
Submission Type
Statement

SNORING CONTROL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963591
510(k) Type
Traditional
Applicant
KENNETH HILSEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1998
Days to Decision
487 days
Submission Type
Statement