Last synced on 2 December 2022 at 11:04 pm

COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022023
510(k) Type
Traditional
Applicant
CLINICAL INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2003
Days to Decision
201 days
Submission Type
Summary

COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022023
510(k) Type
Traditional
Applicant
CLINICAL INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2003
Days to Decision
201 days
Submission Type
Summary