Last synced on 25 January 2026 at 3:41 am

O.N.A.T.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820175
510(k) Type
Traditional
Applicant
LATEX MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
8 days

O.N.A.T.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820175
510(k) Type
Traditional
Applicant
LATEX MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
8 days