The following data is part of a premarket notification filed by Revmedx, Inc. with the FDA for Xstat 30, 3-pack, Xstat 30, 1-pack.
Device ID | K152624 |
510k Number | K152624 |
Device Name: | XSTAT 30, 3-PACK, XSTAT 30, 1-PACK |
Classification | Non-absorbable, Expandable, Hemostatic Sponge For Temporary Internal Use |
Applicant | REVMEDX, INC. 25999 SW CANYON CREEK ROAD, SUITE C Wilsonville, OR 97070 |
Contact | Amy K. Pointer |
Correspondent | John J. Smith HOGAN LOVELLS US LLP 555 THIRTEENTH ST, NW Washington, DC 20004 |
Product Code | PGZ |
CFR Regulation Number | 878.4452 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-14 |
Decision Date | 2015-12-07 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10851587006056 | K152624 | 000 |