Last synced on 30 September 2022 at 11:05 pm

ELECTRO-GONIOMETER DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901290
510(k) Type
Traditional
Applicant
CHATTANOOGA GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1990
Days to Decision
195 days

ELECTRO-GONIOMETER DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901290
510(k) Type
Traditional
Applicant
CHATTANOOGA GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1990
Days to Decision
195 days