Last synced on 27 May 2022 at 11:05 pm

SALTERLABS 8660 SERIES NEBULIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962879
510(k) Type
Traditional
Applicant
SALTER LABS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1996
Days to Decision
90 days
Submission Type
Summary

SALTERLABS 8660 SERIES NEBULIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962879
510(k) Type
Traditional
Applicant
SALTER LABS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1996
Days to Decision
90 days
Submission Type
Summary