Last synced on 25 April 2025 at 11:05 pm

LAPAROSCOPIC ELECTRODE, REUSABLE INDICATOR SHAFT (LERIS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040699
510(k) Type
Traditional
Applicant
MEGADYNE MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2004
Days to Decision
79 days
Submission Type
Summary

LAPAROSCOPIC ELECTRODE, REUSABLE INDICATOR SHAFT (LERIS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040699
510(k) Type
Traditional
Applicant
MEGADYNE MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2004
Days to Decision
79 days
Submission Type
Summary