Company ยท CA
Andromed, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2005. 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 |
|---|---|---|---|
| Sep 30, 2005 | K051779 | ANDROFLOW - RESPIRATORY RATE MONITOR Andromed, Inc., CA | BZQ |
| Oct 1, 2002 | K022298 | I-STETHOS LINK Andromed, Inc., CA | DQD |
| Oct 1, 2002 | K021389 | BIOLOGICAL SOUND MONITOR (BSM) SENSOR Andromed, Inc., CA | DQD |
| Oct 26, 2001 | K010729 | AGILENT ELECTRONIC STETHOSCOPE, MODELS M4532A AND M4533A Andromed, Inc., CA | DQD |
| Jul 20, 2000 | K001306 | STETHOS, MODEL STXXYYZZ OR 001 XXX, STETHOS LINK, MODEL SLXXYYZZ OR 002 XXX Andromed, Inc., CA | DQD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||