The following data is part of a premarket notification filed by Nidek, Inc. with the FDA for Nidek Lm-870 Automatic Lensmeter.
| Device ID | K884188 |
| 510k Number | K884188 |
| Device Name: | NIDEK LM-870 AUTOMATIC LENSMETER |
| Classification | Instrument, Measuring, Lens, Ac-powered |
| Applicant | NIDEK, INC. 2460 EMBARCADERO WAY P.O.BOX 50488 Palo Alto, CA 94303 |
| Contact | Ken Kato |
| Correspondent | Ken Kato NIDEK, INC. 2460 EMBARCADERO WAY P.O.BOX 50488 Palo Alto, CA 94303 |
| Product Code | HLM |
| CFR Regulation Number | 886.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-10-05 |
| Decision Date | 1988-11-23 |