Last synced on 9 May 2025 at 11:05 pm

MOBIL XR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781705
510(k) Type
Traditional
Applicant
SIEMENS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/1978
Days to Decision
14 days

MOBIL XR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781705
510(k) Type
Traditional
Applicant
SIEMENS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/1978
Days to Decision
14 days