The following data is part of a premarket notification filed by Cadwell Laboratories, Inc. with the FDA for Four-channel Preamplifier.
Device ID | K962455 |
510k Number | K962455 |
Device Name: | FOUR-CHANNEL PREAMPLIFIER |
Classification | Stimulator, Electrical, Evoked Response |
Applicant | CADWELL LABORATORIES, INC. 909 NORTH KELLOGG ST. Kennewick, WA 99336 |
Contact | Carlton M Cadwell |
Correspondent | Carlton M Cadwell CADWELL LABORATORIES, INC. 909 NORTH KELLOGG ST. Kennewick, WA 99336 |
Product Code | GWF |
CFR Regulation Number | 882.1870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-06-25 |
Decision Date | 1997-01-13 |
Summary: | summary |