Atlas FDA

AUTO REF-KERATOMETER, RK-3

FDA 510(k) clearance K942242 · decided 1994-09-02

Clearance details

K-number
K942242
Device name
AUTO REF-KERATOMETER, RK-3
Applicant
Cannon U.S.A., Inc.
Decision
Substantially Equivalent
Date received
1994-05-09
Decision date
1994-09-02
Days to decision
116 days
Clearance type
Traditional
Product code
HKO
Device class
1
Regulation number
886.1760
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Lake Success, NY, 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
TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEM (K031831)Topcon Medical Systems, Inc.2003-12-19
WAVESCAN WAVEFRONT SYSTEM MODEL HS 1 (K000327)Visx, Incorporated2000-05-02
DIGITAL RETINOSCOPIC PHOTOMETER (K951179)Kudi Kalu, Inc.1995-05-30
VIDEO VISION ANALYZER (VIVA), VRB 100 (K945959)Tomey Corporation USA1995-03-01
AUTO REFF-30 (K940516)Canon, Inc.1994-07-12
AUTOREF LENSMETER RL-10 (K925304)Canon USA, Inc.1994-02-17
OPTEC 3000 (K924741)Stereo Optical Co., Inc.1993-04-06
BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8 (K924778)R.H. Burton Co.1993-04-05
BURTON AUTO REFRACTOR - MODEL BAR-7 (K924790)R.H. Burton Co.1993-04-05
OPTEC 2300 AFVT, ARMED FORCES VISION TESTER (K904828)Stereo Optical Co., Inc.1991-01-18
AR-1600G AUTO-REFRACTOMETER (K902500)Nidek, Inc.1990-07-27
SHIN NIPPON AUTO REFRACTOMETER QR-007N (K901583)Soderberg, Inc.1990-06-22

Recalls involving this device

No recalls on record reference this clearance.