Last synced on 10 January 2025 at 11:05 pm

Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233644
510(k) Type
Traditional
Applicant
Megadyne Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2024
Days to Decision
242 days
Submission Type
Summary

Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233644
510(k) Type
Traditional
Applicant
Megadyne Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2024
Days to Decision
242 days
Submission Type
Summary