The following data is part of a premarket notification filed by Olympic Medical Corp. with the FDA for Olympic Medical Lectromed Cerebral Function Monitor System, Model 5330.
Device ID | K020335 |
510k Number | K020335 |
Device Name: | OLYMPIC MEDICAL LECTROMED CEREBRAL FUNCTION MONITOR SYSTEM, MODEL 5330 |
Classification | Reduced- Montage Standard Electroencephalograph |
Applicant | OLYMPIC MEDICAL CORP. 5900 FIRST AVE., SOUTH Seattle, WA 98108 |
Contact | Edward B (ted) Weiler |
Correspondent | Edward B (ted) Weiler OLYMPIC MEDICAL CORP. 5900 FIRST AVE., SOUTH Seattle, WA 98108 |
Product Code | OMC |
CFR Regulation Number | 882.1400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-02-01 |
Decision Date | 2002-06-18 |
Summary: | summary |