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CUTTER, P605 GENERAL PURPOSE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770304
510(k) Type
Traditional
Applicant
DENTRONIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
21 days

CUTTER, P605 GENERAL PURPOSE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770304
510(k) Type
Traditional
Applicant
DENTRONIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
21 days