Last synced on 12 August 2022 at 11:05 pm

NITRONOX(R), FIRST RESPONSE NITRONOX(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883833
510(k) Type
Traditional
Applicant
MATRIX MEDICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1989
Days to Decision
161 days

NITRONOX(R), FIRST RESPONSE NITRONOX(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883833
510(k) Type
Traditional
Applicant
MATRIX MEDICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1989
Days to Decision
161 days