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AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)

Page Type
Cleared 510(K)
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)
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