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OHIO NON-REUSABLE TRACHEAL TUBE MURPHY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812879
510(k) Type
Traditional
Applicant
AIRCO/OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1981
Days to Decision
41 days

OHIO NON-REUSABLE TRACHEAL TUBE MURPHY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812879
510(k) Type
Traditional
Applicant
AIRCO/OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1981
Days to Decision
41 days