Last synced on 4 February 2023 at 10:33 pm

GOLDLENS(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913239
510(k) Type
Traditional
Applicant
DORAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1992
Days to Decision
193 days
Submission Type
Statement

GOLDLENS(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913239
510(k) Type
Traditional
Applicant
DORAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1992
Days to Decision
193 days
Submission Type
Statement