Last synced on 20 December 2024 at 11:05 pm

CRITERION I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834274
510(k) Type
Traditional
Applicant
TIMETER INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1984
Days to Decision
127 days

CRITERION I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834274
510(k) Type
Traditional
Applicant
TIMETER INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1984
Days to Decision
127 days