The following data is part of a premarket notification filed by Eurospital S.p.a. with the FDA for Calprest.
Device ID | K130945 |
510k Number | K130945 |
Device Name: | CALPREST |
Classification | Calprotectin, Fecal |
Applicant | EUROSPITAL S.P.A. 3331 EAGLE WATCH DRIVE Woodstock, GA 30189 |
Contact | David Dunn |
Correspondent | David Dunn EUROSPITAL S.P.A. 3331 EAGLE WATCH DRIVE Woodstock, GA 30189 |
Product Code | NXO |
CFR Regulation Number | 866.5180 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-04-04 |
Decision Date | 2014-01-16 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08028169204093 | K130945 | 000 |