Last synced on 20 December 2024 at 11:05 pm

TECHNOMED PULSOLITH LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895178
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1989
Days to Decision
57 days

TECHNOMED PULSOLITH LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895178
510(k) Type
Traditional
Applicant
TEKNOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1989
Days to Decision
57 days