Company ยท US
Non-Invasive Monitoring Systems, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2001. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
2recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 21, 2001 | K012020 | RESPIEVENTS SOFTWARE IS EVENT DATA PROCESSING SOFWARE FOR A PC Non-Invasive Monitoring Systems, Inc. | DQK |
| Jul 26, 2000 | K001369 | RESPIEVENTS, VERSION 4.2 Non-Invasive Monitoring Systems, Inc. | DQK |
| Feb 13, 1996 | K942852 | RESPITRACE PT Non-Invasive Monitoring Systems, Inc. | DQK |
| Feb 13, 1996 | K942771 | RESPIEVENTS Non-Invasive Monitoring Systems, Inc. | DQK |
| Mar 29, 1991 | K903011 | RESPITRACE PLUS, RESPIBANDS, AND RESPICENTRAL Non-Invasive Monitoring Systems, Inc. | BZQ |
| Jun 8, 1989 | K884959 | RESPITRAK Non-Invasive Monitoring Systems, Inc. | BZK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 18, 2012 | Non-Invasive Monitoring Systems, Inc. USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Terminated |
IRO | None listed |
| Jun 18, 2012 | Non-Invasive Monitoring Systems, Inc. US-001 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Terminated |
IRO | None listed |