Last synced on 19 July 2024 at 11:05 pm

FLEX TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881230
510(k) Type
Traditional
Applicant
INTERTECH RESOURCES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1988
Days to Decision
23 days

FLEX TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881230
510(k) Type
Traditional
Applicant
INTERTECH RESOURCES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1988
Days to Decision
23 days