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TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802978
510(k) Type
Traditional
Applicant
BRATTLE INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1981
Days to Decision
73 days

TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802978
510(k) Type
Traditional
Applicant
BRATTLE INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1981
Days to Decision
73 days