The following data is part of a premarket notification filed by Intl. Acoustics, Inc. with the FDA for Modified Dsp100 Amplifier.
Device ID | K873640 |
510k Number | K873640 |
Device Name: | MODIFIED DSP100 AMPLIFIER |
Classification | Phonocardiograph |
Applicant | INTL. ACOUSTICS, INC. 1250 W. NORTHWEST HIGHWAY, SUITE 720 Palatine, IL 60067 |
Contact | Kien, Phd |
Correspondent | Kien, Phd INTL. ACOUSTICS, INC. 1250 W. NORTHWEST HIGHWAY, SUITE 720 Palatine, IL 60067 |
Product Code | DQC |
CFR Regulation Number | 870.2390 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-09-09 |
Decision Date | 1987-12-07 |