Last synced on 30 September 2022 at 11:05 pm

KT-1000 DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812806
510(k) Type
Traditional
Applicant
MEDMETRIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1981
Days to Decision
35 days

KT-1000 DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812806
510(k) Type
Traditional
Applicant
MEDMETRIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1981
Days to Decision
35 days