Last synced on 2 December 2022 at 11:04 pm

TRI-MED QUICK-STEP(TM) RECTAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924549
510(k) Type
Traditional
Applicant
TRI-MED SPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1994
Days to Decision
519 days
Submission Type
Statement

TRI-MED QUICK-STEP(TM) RECTAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924549
510(k) Type
Traditional
Applicant
TRI-MED SPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1994
Days to Decision
519 days
Submission Type
Statement