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FDA 510(k)

CANON AUTOREFRACTOMETER R-20

K-Number: K882287 · 1988-07-01

ApplicantCanon USA, Inc.
Decision Date1988-07-01
Product CodeHKO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CANON AUTOREFRACTOMETER R-20 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 1988-07-01 under 510(k) number K882287. 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 CANON AUTOREFRACTOMETER R-20?

CANON AUTOREFRACTOMETER R-20 is a medical device that received FDA 510(k) clearance on 1988-07-01. The listed applicant is Canon USA, Inc.. The 510(k) number is K882287.

When did CANON AUTOREFRACTOMETER R-20 receive FDA 510(k) clearance?

CANON AUTOREFRACTOMETER R-20 received FDA 510(k) clearance on 1988-07-01, under 510(k) number K882287.

Who is the listed applicant for CANON AUTOREFRACTOMETER R-20?

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 CANON AUTOREFRACTOMETER R-20?

The FDA product code for CANON AUTOREFRACTOMETER R-20 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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