Last synced on 24 June 2022 at 11:05 pm

SAFE-T-TUBE RADIOPAQUE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930150
510(k) Type
Traditional
Applicant
BOSTON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
39 days
Submission Type
Statement

SAFE-T-TUBE RADIOPAQUE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930150
510(k) Type
Traditional
Applicant
BOSTON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
39 days
Submission Type
Statement