Last synced on 30 September 2022 at 11:05 pm

PARIETEX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982532
510(k) Type
Traditional
Applicant
COGENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1999
Days to Decision
184 days
Submission Type
Summary

PARIETEX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982532
510(k) Type
Traditional
Applicant
COGENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1999
Days to Decision
184 days
Submission Type
Summary