Company ยท US
Schiller America, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1998. Name variants (Inc, Corp, punctuation) are merged.
10510(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 |
|---|---|---|---|
| Aug 25, 1998 | K973751 | MT-200 Schiller America, Inc. | DQK |
| Aug 25, 1998 | K973735 | MICROVIT MT-100 Schiller America, Inc. | DSH |
| Jun 25, 1997 | K970879 | CARDIOVIT CS-200 Schiller America, Inc. | LOS |
| Dec 19, 1995 | K953396 | CARDIOVIT AT-1C, AT-2C Schiller America, Inc. | LOS |
| Oct 27, 1995 | K954066 | MINISCOPE MS-3 Schiller America, Inc. | DPS |
| May 19, 1995 | K941462 | CARDIOVIT AT-5C Schiller America, Inc. | LOS |
| Mar 16, 1995 | K946205 | CARDIOVIT AT-1, P-80 Schiller America, Inc. | DPS |
| Nov 3, 1992 | K914970 | CARDIOVIT CS-100 Schiller America, Inc. | LOS |
| Jan 9, 1990 | K896121 | SCHILLER MODEL SP-200 SPIROVIT(TM) Schiller America, Inc. | BZG |
| Jan 9, 1990 | K896120 | SCHILLER MODEL SP-100 SPIROVIT(TM) Schiller America, Inc. | BZG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||