Last synced on 20 January 2023 at 11:05 pm

AIRVIT MODEL 8500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843594
510(k) Type
Traditional
Applicant
LASERMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/1985
Days to Decision
211 days

AIRVIT MODEL 8500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843594
510(k) Type
Traditional
Applicant
LASERMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/1985
Days to Decision
211 days