Last synced on 23 May 2025 at 11:06 pm

TANDEM E GCG VISUAL END POINT INNUMOENZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830138
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1983
Days to Decision
25 days

TANDEM E GCG VISUAL END POINT INNUMOENZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830138
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1983
Days to Decision
25 days