The following data is part of a premarket notification filed by Hyperion, Inc. with the FDA for Micro-reader.
Device ID | K864060 |
510k Number | K864060 |
Device Name: | MICRO-READER |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
Applicant | HYPERION, INC. 14100 S.W. 136TH ST. Miami, FL 33186 |
Contact | Harter |
Correspondent | Harter HYPERION, INC. 14100 S.W. 136TH ST. Miami, FL 33186 |
Product Code | JJQ |
CFR Regulation Number | 862.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-10-20 |
Decision Date | 1986-11-28 |