Last synced on 23 May 2025 at 11:06 pm

PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010824
510(k) Type
Traditional
Applicant
SCIENCE INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2001
Days to Decision
78 days
Submission Type
Summary

PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010824
510(k) Type
Traditional
Applicant
SCIENCE INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2001
Days to Decision
78 days
Submission Type
Summary