Last synced on 30 May 2025 at 11:05 pm

GIKTER ECG CASSETTE TAPE RECORDER MODEL XR 300

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921068
510(k) Type
Traditional
Applicant
DATRIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1992
Days to Decision
24 days
Submission Type
Statement

GIKTER ECG CASSETTE TAPE RECORDER MODEL XR 300

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921068
510(k) Type
Traditional
Applicant
DATRIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1992
Days to Decision
24 days
Submission Type
Statement