FDA 510(k) Applications Submitted by BARBARA STEGMEIER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100305 | 02/03/2010 | ETURN SPINAL IMPLANT MODEL ETURN XX-12; ETURN XX-16 WHERE XX=07, 09, 11, 13, OR 15 AND ETURN XX-12 K; ETURN XX-16 K WHER | ICOTEC |
| K042281 | 08/24/2004 | MODIFICATION TO ACCESS HYPERSENSITIVE HTSH ASSAY | BECKMAN COULTER, INC. |
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