The following data is part of a premarket notification filed by Corning Medical & Scientific with the FDA for Ph Meter-125 (.01 Ph).
Device ID | K760788 |
510k Number | K760788 |
Device Name: | PH METER-125 (.01 PH) |
Classification | Ph Meter |
Applicant | CORNING MEDICAL & SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JQY |
CFR Regulation Number | 862.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1976-09-10 |
Decision Date | 1976-11-16 |