Last synced on 25 November 2022 at 11:04 pm

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760452
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1976
Days to Decision
14 days

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760452
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1976
Days to Decision
14 days