Last synced on 25 January 2026 at 3:41 am

NEOLEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011564
510(k) Type
Traditional
Applicant
Neotech Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2002
Days to Decision
227 days
Submission Type
Summary

NEOLEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011564
510(k) Type
Traditional
Applicant
Neotech Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2002
Days to Decision
227 days
Submission Type
Summary