Last synced on 14 November 2025 at 11:06 pm

INTRODUCER FOR ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
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)
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