The following data is part of a premarket notification filed by Randwal Instrument Co., Inc. with the FDA for Iras Perimeter.
Device ID | K864012 |
510k Number | K864012 |
Device Name: | IRAS PERIMETER |
Classification | Instrument, Visual Field, Laser |
Applicant | RANDWAL INSTRUMENT CO., INC. 278 WORCESTER ST. Southbridge, MA 01550 |
Contact | Remijan, Ph.d. |
Correspondent | Remijan, Ph.d. RANDWAL INSTRUMENT CO., INC. 278 WORCESTER ST. Southbridge, MA 01550 |
Product Code | HPJ |
CFR Regulation Number | 886.1360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-10-15 |
Decision Date | 1986-12-12 |