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AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960309
510(k) Type
Traditional
Applicant
AIRSEP CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1997
Days to Decision
420 days
Submission Type
Statement

AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960309
510(k) Type
Traditional
Applicant
AIRSEP CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1997
Days to Decision
420 days
Submission Type
Statement