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FETALERT ADR FETAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871383
510(k) Type
Traditional
Applicant
ADVANCED TECHNOLOGY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1987
Days to Decision
55 days

FETALERT ADR FETAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871383
510(k) Type
Traditional
Applicant
ADVANCED TECHNOLOGY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1987
Days to Decision
55 days