The following data is part of a premarket notification filed by Niic U.s.a., Inc. with the FDA for Niic Model: Dx901 Aspiration System.
Device ID | K900185 |
510k Number | K900185 |
Device Name: | NIIC MODEL: DX901 ASPIRATION SYSTEM |
Classification | Ph Rate Measurement, Carbon-dioxide |
Applicant | NIIC U.S.A., INC. 460 SEAPORT CT., SUITE 101 Redwood City, CA 94063 |
Contact | Michael Moretti |
Correspondent | Michael Moretti NIIC U.S.A., INC. 460 SEAPORT CT., SUITE 101 Redwood City, CA 94063 |
Product Code | JFL |
CFR Regulation Number | 862.1160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-16 |
Decision Date | 1990-05-24 |