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FUKUDA DENSHI MODEL SPIROSIFT 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900391
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
74 days

FUKUDA DENSHI MODEL SPIROSIFT 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900391
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
74 days