Last synced on 30 September 2022 at 11:05 pm

RELIANCE OPHTHALMIC INSTRUMENT CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812544
510(k) Type
Traditional
Applicant
F. & F. KOENIGKRAMER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1981
Days to Decision
17 days

RELIANCE OPHTHALMIC INSTRUMENT CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812544
510(k) Type
Traditional
Applicant
F. & F. KOENIGKRAMER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1981
Days to Decision
17 days