Last synced on 19 July 2024 at 11:05 pm

SCHILLER MODEL SP-200 SPIROVIT(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896121
510(k) Type
Traditional
Applicant
SCHILLER AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1990
Days to Decision
77 days

SCHILLER MODEL SP-200 SPIROVIT(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896121
510(k) Type
Traditional
Applicant
SCHILLER AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1990
Days to Decision
77 days