Last synced on 1 July 2022 at 11:04 pm

CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101154
510(k) Type
Traditional
Applicant
AIRSEP CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2011
Days to Decision
339 days
Submission Type
Summary

CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101154
510(k) Type
Traditional
Applicant
AIRSEP CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2011
Days to Decision
339 days
Submission Type
Summary