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SYSTEM 86 COMPUTERIZED LUNG VOL. SPIROME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810243
510(k) Type
Traditional
Applicant
CARDIO PULMONARY INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1981
Days to Decision
15 days

SYSTEM 86 COMPUTERIZED LUNG VOL. SPIROME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810243
510(k) Type
Traditional
Applicant
CARDIO PULMONARY INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1981
Days to Decision
15 days