Last synced on 16 August 2024 at 11:05 pm

MODEL TX-8 PANENDOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760822
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1976
Days to Decision
8 days

MODEL TX-8 PANENDOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760822
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1976
Days to Decision
8 days