Last synced on 19 July 2024 at 11:05 pm

DUAL PURPOSE CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833375
510(k) Type
Traditional
Applicant
JINOTTI ENT INC. MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1984
Days to Decision
135 days

DUAL PURPOSE CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833375
510(k) Type
Traditional
Applicant
JINOTTI ENT INC. MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1984
Days to Decision
135 days