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PORTABLE LIQUID OXYGEN UNIT (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863978
510(k) Type
Traditional
Applicant
PENOX TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/1986
Days to Decision
62 days

PORTABLE LIQUID OXYGEN UNIT (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863978
510(k) Type
Traditional
Applicant
PENOX TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/1986
Days to Decision
62 days