The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Attest(tm) Auto-reader.
Device ID | K123546 |
510k Number | K123546 |
Device Name: | 3M ATTEST(TM) AUTO-READER |
Classification | Indicator, Biological Sterilization Process |
Applicant | 3M COMPANY 3M CENTER, BLDG. 275--05-W-06 St. Paul, MN 55144 -1000 |
Contact | Suzanne Leung |
Correspondent | Suzanne Leung 3M COMPANY 3M CENTER, BLDG. 275--05-W-06 St. Paul, MN 55144 -1000 |
Product Code | FRC |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-11-19 |
Decision Date | 2013-03-18 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
50707387767148 | K123546 | 000 |
50707387767131 | K123546 | 000 |