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FDA 510(k)

AUTO REF-KERATOMETER, RK-3

K-Number: K942242 · 1994-09-02

ApplicantCannon U.S.A., Inc.
Decision Date1994-09-02
Product CodeHKO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTO REF-KERATOMETER, RK-3 is the device name listed in this FDA 510(k) record. The listed applicant is Cannon U.S.A., Inc.. It received FDA 510(k) clearance on 1994-09-02 under 510(k) number K942242. The device is classified under product code HKO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO REF-KERATOMETER, RK-3?

AUTO REF-KERATOMETER, RK-3 is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Cannon U.S.A., Inc.. The 510(k) number is K942242.

When did AUTO REF-KERATOMETER, RK-3 receive FDA 510(k) clearance?

AUTO REF-KERATOMETER, RK-3 received FDA 510(k) clearance on 1994-09-02, under 510(k) number K942242.

Who is the listed applicant for AUTO REF-KERATOMETER, RK-3?

The FDA 510(k) record lists Cannon U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO REF-KERATOMETER, RK-3?

The FDA product code for AUTO REF-KERATOMETER, RK-3 is HKO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cannon U.S.A., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960839FILM SCANNER 300

Related Devices (Code: HKO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K031831TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEMTopcon Medical Systems, Inc.K000327WAVESCAN WAVEFRONT SYSTEM MODEL HS 1Visx, IncorporatedK951179DIGITAL RETINOSCOPIC PHOTOMETERKudi Kalu, Inc.K945959VIDEO VISION ANALYZER (VIVA), VRB 100Tomey Corporation USAK940516AUTO REFF-30Canon, Inc.K925304AUTOREF LENSMETER RL-10Canon USA, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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