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TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881303
510(k) Type
Traditional
Applicant
TRITON TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1988
Days to Decision
246 days

TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881303
510(k) Type
Traditional
Applicant
TRITON TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1988
Days to Decision
246 days