Variable Contrast Acuiometer, Diagnostic Laser Interferometer
FDA 510(k) K827577 · Randwal Instrument Co., Inc.
510(k) numberK827577
Submission
- Device name
- Variable Contrast Acuiometer, Diagnostic Laser Interferometer
- Applicant
- Randwal Instrument Co., Inc.
Southbridge, MA, US - Received
- December 20, 1982
- Decision date
- January 24, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Randwal Instrument Co., Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K873990 | Iras Eds Interferometric StimulatorHLX · Traditional | 02/05/1988SE |
| K873987 | Iras Glare TesterHLJ · Traditional | 11/24/1987SE |
| K864012 | Iras PerimeterHPJ · Traditional | 12/12/1986SE |
| K853556 | Laser IrasHPJ · Traditional | 11/01/1985SE |
| K842567 | Portable AcuiometerHLJ · Traditional | 08/15/1984SE |
Questions and answers
When was Variable Contrast Acuiometer, Diagnostic Laser Interferometer cleared by the FDA?
Variable Contrast Acuiometer, Diagnostic Laser Interferometer (K827577) received a 510(k) decision of Substantially Equivalent on January 24, 1983, 35 days after the submission was received.