Last synced on 25 January 2026 at 3:41 am

K-AID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820150
510(k) Type
Traditional
Applicant
SYTEK LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
10 days

K-AID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820150
510(k) Type
Traditional
Applicant
SYTEK LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
10 days