Last synced on 17 March 2023 at 11:04 pm

PROJECTOR, ACCU-CHART ACUITY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781658
510(k) Type
Traditional
Applicant
BAUSCH & LOMB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1978
Days to Decision
19 days

PROJECTOR, ACCU-CHART ACUITY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781658
510(k) Type
Traditional
Applicant
BAUSCH & LOMB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1978
Days to Decision
19 days