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MULTILASE 2100 C, 2100 D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913917
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1992
Days to Decision
429 days
Submission Type
Statement

MULTILASE 2100 C, 2100 D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913917
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1992
Days to Decision
429 days
Submission Type
Statement