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MULTILASE 2500 A

Page Type
Cleared 510(K)
510(k) Number
K920708
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1992
Days to Decision
261 days
Submission Type
Statement

MULTILASE 2500 A

Page Type
Cleared 510(K)
510(k) Number
K920708
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1992
Days to Decision
261 days
Submission Type
Statement