HEARIT— 510(k) K934805
Substantially EquivalentJe Liss & Co., Inc.
FDA 510(k) clearance K934805 for HEARIT, Substantially Equivalent on 1994-02-07. Applicant: Je Liss & Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Je Liss & Co., Inc.
- Product code
- Code LZI
- Device class
- Class 2
- Regulation
- 21 CFR 874.3320
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tucson, AZ, US
Recent devices under product code LZI
view allData sourced from openFDA. This site is unofficial and independent of the FDA.