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BALLOON RETENTION CHEST CATHETER

Page Type
Cleared 510(K)
510(k) Number
K802025
510(k) Type
Traditional
Applicant
LOSEFF MEDICAL DESIGNERS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1980
Days to Decision
37 days

BALLOON RETENTION CHEST CATHETER

Page Type
Cleared 510(K)
510(k) Number
K802025
510(k) Type
Traditional
Applicant
LOSEFF MEDICAL DESIGNERS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1980
Days to Decision
37 days