Last synced on 29 September 2023 at 11:04 pm

ACCORDION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052048
510(k) Type
Traditional
Applicant
PERCUTANEOUS SYSTEMS, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2005
Days to Decision
46 days
Submission Type
Summary

ACCORDION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052048
510(k) Type
Traditional
Applicant
PERCUTANEOUS SYSTEMS, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2005
Days to Decision
46 days
Submission Type
Summary