The following data is part of a premarket notification filed by Trimeter Instrument Corp. with the FDA for Vacuum Regulator 0-2000 Mmhg Vr-1000.
Device ID | K834224 |
510k Number | K834224 |
Device Name: | VACUUM REGULATOR 0-2000 MMHG VR-1000 |
Classification | Regulator, Vacuum |
Applicant | TRIMETER INSTRUMENT CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KDP |
CFR Regulation Number | 880.6740 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-12-06 |
Decision Date | 1984-02-27 |