Last synced on 19 July 2024 at 11:05 pm

MAXI-USE O2 DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861325
510(k) Type
Traditional
Applicant
B & F MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1986
Days to Decision
153 days

MAXI-USE O2 DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861325
510(k) Type
Traditional
Applicant
B & F MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1986
Days to Decision
153 days