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FDA 510(k)

AUTOREF LENSMETER RL-10

K-Number: K925304 · 1994-02-17

ApplicantCanon USA, Inc.
Decision Date1994-02-17
Product CodeHKO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTOREF LENSMETER RL-10 is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K925304. 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 AUTOREF LENSMETER RL-10?

AUTOREF LENSMETER RL-10 is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Canon USA, Inc.. The 510(k) number is K925304.

When did AUTOREF LENSMETER RL-10 receive FDA 510(k) clearance?

AUTOREF LENSMETER RL-10 received FDA 510(k) clearance on 1994-02-17, under 510(k) number K925304.

Who is the listed applicant for AUTOREF LENSMETER RL-10?

The FDA 510(k) record lists Canon USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOREF LENSMETER RL-10?

The FDA product code for AUTOREF LENSMETER RL-10 is HKO.

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Other records listing Canon USA, 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.

K090623DIGITAL RADIOGRAPHY CXDI-40G COMPACTK033624PACS SOFTWARE SOLUTION 2003K031633CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40CK031629CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGIK023750CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40GK023586DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS

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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 USAK942242AUTO REF-KERATOMETER, RK-3Cannon U.S.A., Inc.K940516AUTO REFF-30Canon, 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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