Last synced on 2 May 2025 at 11:05 pm

MODEL 3000 NUCLEAR CAMERA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882312
510(k) Type
Traditional
Applicant
OHIO IMAGING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1988
Days to Decision
41 days

MODEL 3000 NUCLEAR CAMERA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882312
510(k) Type
Traditional
Applicant
OHIO IMAGING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1988
Days to Decision
41 days