FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LORI-CIC HEARING AID

K Number: K940639 · Decision Mar 25, 1994
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
8
Review Days
39

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LORI-CIC HEARING AID
K Number
K940639
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lori Medical Laboratories, Inc.
Date Received
February 14, 1994
Decision Date
March 25, 1994
Product Code
ESD
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ESD Hearing Aid, Air-Conduction, Prescription

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ESD), ordered by most recent decision date.

View all

Other Clearances by Lori Medical Laboratories, Inc.

K Number Device Name
K973376 LORI/LORI, LORI-S (LORI STOCK AID)
K972058 LORIPRO, LORIPRO II
K964080 LORI HEARING AID SIMULATOR
K952711 LORI-A
K893721 LORI-MODEL O, LOW PROFILE IN-THE EAR INSTRUMENT
K893722 LORI-MODEL H, HALF CONCHA IN-THE-EAR INSTRUMENT
K893723 LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT