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KINETIX MOUTHPIECE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833420
510(k) Type
Traditional
Applicant
KINETIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1984
Days to Decision
99 days

KINETIX MOUTHPIECE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833420
510(k) Type
Traditional
Applicant
KINETIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1984
Days to Decision
99 days