The following data is part of a premarket notification filed by Yellow Springs Instrument Co., Inc. with the FDA for Ysi #2600 Multi-channel Dual-display.
Device ID | K823231 |
510k Number | K823231 |
Device Name: | YSI #2600 MULTI-CHANNEL DUAL-DISPLAY |
Classification | Analyzer, Gas, Oxygen, Gaseous-phase |
Applicant | YELLOW SPRINGS INSTRUMENT CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CCL |
CFR Regulation Number | 868.1720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-10-29 |
Decision Date | 1982-12-07 |