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INTRODUCER FOR ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820451
510(k) Type
Traditional
Applicant
IMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/1982
Days to Decision
36 days

INTRODUCER FOR ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820451
510(k) Type
Traditional
Applicant
IMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/1982
Days to Decision
36 days