Last synced on 19 July 2024 at 11:05 pm

MODEL 3862A & B 3863A & B TEMP. LEAD SCREENING KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932202
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1994
Days to Decision
363 days
Submission Type
Summary

MODEL 3862A & B 3863A & B TEMP. LEAD SCREENING KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932202
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1994
Days to Decision
363 days
Submission Type
Summary