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FDA 510(k)

AUTOREFRACTOR, SUBJECTIVE

K-Number: K781014 · 1978-09-07

ApplicantCavitron Corp.
Decision Date1978-09-07
Product CodeHKO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTOREFRACTOR, SUBJECTIVE is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1978-09-07 under 510(k) number K781014. 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 AUTOREFRACTOR, SUBJECTIVE?

AUTOREFRACTOR, SUBJECTIVE is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Cavitron Corp.. The 510(k) number is K781014.

When did AUTOREFRACTOR, SUBJECTIVE receive FDA 510(k) clearance?

AUTOREFRACTOR, SUBJECTIVE received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781014.

Who is the listed applicant for AUTOREFRACTOR, SUBJECTIVE?

The FDA 510(k) record lists Cavitron Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOREFRACTOR, SUBJECTIVE?

The FDA product code for AUTOREFRACTOR, SUBJECTIVE is HKO.

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Other records listing Cavitron Corp. 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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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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