The following data is part of a premarket notification filed by Datascope Corp. with the FDA for Datascope Multinex Id Monitor.
Device ID | K910106 |
510k Number | K910106 |
Device Name: | DATASCOPE MULTINEX ID MONITOR |
Classification | Analyzer, Gas, Carbon-dioxide, Gaseous-phase |
Applicant | DATASCOPE CORP. 580 WINTERS AVE. P.O. BOX 5 Paramus, NJ 07653 |
Contact | Amrik Sikand |
Correspondent | Amrik Sikand DATASCOPE CORP. 580 WINTERS AVE. P.O. BOX 5 Paramus, NJ 07653 |
Product Code | CCK |
CFR Regulation Number | 868.1400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-01-10 |
Decision Date | 1991-03-29 |