Last synced on 30 September 2022 at 11:05 pm

S 22 INSTRUMENT STAND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891584
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1989
Days to Decision
80 days

S 22 INSTRUMENT STAND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891584
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1989
Days to Decision
80 days