FDA 510(k) Applications Submitted by SURGIN SURGICAL INSTRUMENTATION, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980849 |
02/05/1998 |
SURGIN KIT |
SURGIN SURGICAL INSTRUMENTATION, INC. |
| K011195 |
04/19/2001 |
PRIZM BLADE (MORIA MODEL) LSK / MK8510LSK; PRIZM BLADE (MORIA MODEL) CB / MK8511CB |
SURGIN SURGICAL INSTRUMENTATION, INC. |
| K033182 |
10/01/2003 |
PRIZM KERATOME BLADE (B.D. MODEL), MODEL MK8530BD |
SURGIN SURGICAL INSTRUMENTATION, INC. |
| K033236 |
10/06/2003 |
PRIZM KERATOME BLADE, MODEL MK8512M2 |
SURGIN SURGICAL INSTRUMENTATION, INC. |
| K994015 |
11/26/1999 |
ACCUBLADE (ACS MODEL), MK8507, ACCUBLADE (HANSOTOME MODEL), MK8508 |
SURGIN SURGICAL INSTRUMENTATION, INC. |
| K082110 |
07/28/2008 |
DUAL SYRINGE HOLDER |
SURGIN SURGICAL INSTRUMENTATION, INC. |
|
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