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UMBILICAL CORD BLOOD SAMPLING KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900302
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
78 days

UMBILICAL CORD BLOOD SAMPLING KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900302
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
78 days