Last synced on 25 January 2026 at 3:41 am

BUCKYMAT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790069
510(k) Type
Traditional
Applicant
SIEMENS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1979
Days to Decision
14 days

BUCKYMAT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790069
510(k) Type
Traditional
Applicant
SIEMENS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1979
Days to Decision
14 days