FDA 510(k) Applications Submitted by REMEL, L.P.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K964315 |
10/29/1996 |
REMEL STAPH LATEX KIT |
REMEL, L.P. |
| K955136 |
11/13/1995 |
RPR CARD TEST KIT |
REMEL, L.P. |
| K955143 |
11/13/1995 |
RPR LIQUID CONTROLS |
REMEL, L.P. |
| K964421 |
10/01/1996 |
REMEL MEROPENEM 10UG SUSCEPTIBILITY DISK |
REMEL, L.P. |
| K960313 |
01/22/1996 |
MUELLER HINTON AGAR WITH 2% NACI |
REMEL, L.P. |
| K961046 |
03/15/1996 |
10B ARGININE BROTH |
REMEL, L.P. |
| K961818 |
05/10/1996 |
GENTAMICIN DISK (120MCG) |
REMEL, L.P. |
| K961819 |
05/10/1996 |
STREPTOMYCIN DISK (300MCG) |
REMEL, L.P. |
| K972359 |
06/25/1997 |
REMEL BILE ESCULIN AZIDE AGAR W/6 MCG/ML VANCOMYCIN |
REMEL, L.P. |
| K954986 |
10/31/1995 |
GC BASE W/ 1% GCHI |
REMEL, L.P. |
|
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