Atlas FDA

RASTRONICS CCI 8

FDA 510(k) clearance K902244 · decided 1990-10-05

Clearance details

K-number
K902244
Device name
RASTRONICS CCI 8
Applicant
Rastronics USA, Inc.
Decision
Substantially Equivalent
Date received
1990-05-18
Decision date
1990-10-05
Days to decision
140 days
Clearance type
Traditional
Product code
ETW
Device class
2
Regulation number
874.3310
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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FONIX, MODEL 7000 (K022510)Frye Electronics, Inc.2002-08-27
AUDIOSCAN VERIFIT, MODEL VF-1 (K012306)Etymonic Design, Inc.2001-09-21
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Recalls involving this device

No recalls on record reference this clearance.