The following data is part of a premarket notification filed by Mettler Electronics Corp. with the FDA for Silberg T.p.s., Tissue Preparation System, Model Me 800.
Device ID | K023083 |
510k Number | K023083 |
Device Name: | SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800 |
Classification | Pump, Infusion |
Applicant | METTLER ELECTRONICS CORP. 1333 SOUTH CLAUDINA ST. Anaheim, CA 92805 |
Contact | Robert E Fleming |
Correspondent | Robert E Fleming METTLER ELECTRONICS CORP. 1333 SOUTH CLAUDINA ST. Anaheim, CA 92805 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Se Subject To Tracking Reg (ST) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-09-17 |
Decision Date | 2003-02-28 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00816864020432 | K023083 | 000 |