The following data is part of a premarket notification filed by Singer Medical Products, Inc. with the FDA for Impedance Analyzer Models Md-2, Md-p.
Device ID | K895783 |
510k Number | K895783 |
Device Name: | IMPEDANCE ANALYZER MODELS MD-2, MD-P |
Classification | Tester, Auditory Impedance |
Applicant | SINGER MEDICAL PRODUCTS, INC. 790 MAPLE LN. Bensenville, IL 60106 |
Contact | James I Beck |
Correspondent | James I Beck SINGER MEDICAL PRODUCTS, INC. 790 MAPLE LN. Bensenville, IL 60106 |
Product Code | ETY |
CFR Regulation Number | 874.1090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-07-26 |
Decision Date | 1989-12-05 |