Company ยท US
Siemens Burdick, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1992. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Oct 9, 1992 | K915327 | ELITE II ELECTROCARDIOGRAPH,MODIFIED Siemens Burdick, Inc. | LOS |
| Jul 1, 1992 | K915225 | MEGACART Siemens Burdick, Inc. | LOS |
| May 15, 1992 | K915202 | INTERNAL MODEM FOR THE E560 ELECTROCARDIOGRAPH Siemens Burdick, Inc. | LOS |
| Mar 26, 1992 | K914969 | E350I ELECTROCARDIOGRAPH Siemens Burdick, Inc. | LOS |
| Oct 24, 1991 | K913518 | TA620 TREADMILL CONTROLLER Siemens Burdick, Inc. | IOL |
| Jul 24, 1991 | K910634 | DC200 DEFIBRILLATOR Siemens Burdick, Inc. | LDD |
| May 31, 1991 | K910867 | T600 TREADMILL Siemens Burdick, Inc. | IOL |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||