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TECHNOMED PULSOLITH LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K890436
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1989
Days to Decision
55 days

TECHNOMED PULSOLITH LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K890436
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1989
Days to Decision
55 days