FDA 510(k) Applications Submitted by LISA PEACOCK
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K110288 |
02/01/2011 |
FEMVUE SALINE-AIR DEVICE |
FEMASYS INC. |
| K100662 |
03/08/2010 |
FEMVUE CORNUAL BALLOON CATHETER |
FEMASYS INC. |
| K110993 |
04/08/2011 |
FEMCHEC PRESSURE MANAGEMET DEVICE |
FEMASYS INC. |
| K091685 |
06/10/2009 |
KIMGUARD ONE-STEP STERILIZATION WRAP, MODELS KC100, KC200, KC300, KC400, KC 500, KC600 |
KIMBERLY-CLARK CORP. |
| K082177 |
08/01/2008 |
KIMGUARD ONE-STEP STERILIZATION WRAP |
KIMBERLY-CLARK CORP. |
| K122658 |
08/31/2012 |
FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009 |
FEMASYS INC. |
| K082554 |
09/03/2008 |
KIMGUARD STERILIZATION WRAP, MODELS KC100, KC200, KC300, KC400, KC500 AND KC600 |
KIMBERLY-CLARK CORP. |
| K083234 |
11/03/2008 |
KIMBERLY-CLARK KC100 SURGICAL DRAPES, MODEL KC 100, KIMBERLY-CLARK KC100 SURGICAL EQUIPMENT COVERS, MODEL KC 100 |
KIMBERLY-CLARK CORP. |
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