Atlas FDA

KANIEVSKI SENSORY AID OR DEVICE

FDA 510(k) clearance K843433 · decided 1984-11-14

Clearance details

K-number
K843433
Device name
KANIEVSKI SENSORY AID OR DEVICE
Applicant
Spectro Industries, Inc.
Decision
Substantially Equivalent
Date received
1984-09-04
Decision date
1984-11-14
Days to decision
71 days
Clearance type
Traditional
Product code
LRA
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Jenkintown, PA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ETA (K883853)Sevrain-Tech, Inc.1988-11-17
WEARABLE TWENTY-FOUR CHANNEL VIBROTACTILE VOCODER (K862471)Institute of Logopedics1986-09-12
TACTICON 1600 (K851441)Medecon1985-06-27
TEACHER TM (K851655)Monargue Intl.1985-06-20
TACTIL EAR (K831501)Ear Three Systems1983-08-26
TACTAID (K830418)Audiological Engineering Corp.1983-03-10
VIBRO-COM COMMUNICATOR #8827 (K813057)Sonic Systems, Inc.1981-12-02

Recalls involving this device

No recalls on record reference this clearance.