Last synced on 12 October 2025 at 8:21 pm

ECG MODULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922412
510(k) Type
Traditional
Applicant
MAGUIRE ENT., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1992
Days to Decision
46 days
Submission Type
Statement

ECG MODULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922412
510(k) Type
Traditional
Applicant
MAGUIRE ENT., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1992
Days to Decision
46 days
Submission Type
Statement