Last synced on 14 November 2025 at 11:06 pm

DORNIER LASER LITHOTRIPTER IMPACT

Page Type
Cleared 510(K)
510(k) Number
K913191
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1991
Days to Decision
90 days
Submission Type
Statement

DORNIER LASER LITHOTRIPTER IMPACT

Page Type
Cleared 510(K)
510(k) Number
K913191
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1991
Days to Decision
90 days
Submission Type
Statement