The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Elecsys Psa (on Elecsys 1010).
Device ID | K974189 |
510k Number | K974189 |
Device Name: | ELECSYS PSA (ON ELECSYS 1010) |
Classification | Prostate-specific Antigen (psa) For Management Of Prostate Cancers |
Applicant | BOEHRINGER MANNHEIM CORP. 4300 HACIENDA DR. Pleasanton, CA 94588 -2722 |
Contact | Patricia M Klimley |
Correspondent | Patricia M Klimley BOEHRINGER MANNHEIM CORP. 4300 HACIENDA DR. Pleasanton, CA 94588 -2722 |
Product Code | LTJ |
CFR Regulation Number | 866.6010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-11-07 |
Decision Date | 1998-01-06 |
Summary: | summary |