Company ยท US
Healthdyne Cardiovascular, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1990. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 25, 1990 | K901643 | ISOFLO(TM) AMNIOCENTESIS TRAY Healthdyne Cardiovascular, Inc. | HIO |
| Jul 19, 1990 | K901382 | ISOFLO(TM) HIGH PRESSURE INJECTION LINES Healthdyne Cardiovascular, Inc. | DXT |
| Jun 1, 1990 | K901084 | ISOFLO INTRAUTERINE PRESSURE MONITORING & AMNIO. Healthdyne Cardiovascular, Inc. | KXO |
| May 14, 1990 | K900665 | DRESSING CHANGE KIT Healthdyne Cardiovascular, Inc. | FXX |
| Dec 22, 1989 | K895763 | ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING Healthdyne Cardiovascular, Inc. | KXO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||