FDA 510(k) Applications Submitted by GALLINI U.S., LLC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980248 |
01/23/1998 |
ACRI R NEEDLE |
GALLINI U.S., LLC. |
| K980479 |
02/06/1998 |
QUICK-CUT AUTOMATIC BIOPSY SYSTEM |
GALLINI U.S., LLC. |
| K980676 |
02/20/1998 |
SPIGAL NEEDLE |
GALLINI U.S., LLC. |
| K990645 |
02/26/1999 |
GALLINI ATRA-CUT NEEDLE |
GALLINI U.S., LLC. |
| K990716 |
03/04/1999 |
GALLINI BYCUT NEEDLE |
GALLINI U.S., LLC. |
| K981301 |
04/09/1998 |
SPEED-CUT AUTOMATIC BIOPSY SYSTEM |
GALLINI U.S., LLC. |
| K972266 |
06/17/1997 |
GALLINI COAXIAL INTRODUCER |
GALLINI U.S., LLC. |
| K992499 |
07/26/1999 |
GALLINI BIOSYSTEM BONE MARROW ASPIRATION/BIOPSY NEEDLE |
GALLINI U.S., LLC. |
| K973152 |
08/22/1997 |
GALLINI ABS DEVICE |
GALLINI U.S., LLC. |
| K974440 |
11/25/1997 |
IBI |
GALLINI U.S., LLC. |
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