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FDA 510(k)

EYE SEE INSTRUMENT

K-Number: K905237 · 1991-02-14

ApplicantKing Tool, Inc.
Decision Date1991-02-14
Product CodeHPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EYE SEE INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is King Tool, Inc.. It received FDA 510(k) clearance on 1991-02-14 under 510(k) number K905237. The device is classified under product code HPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EYE SEE INSTRUMENT?

EYE SEE INSTRUMENT is a medical device that received FDA 510(k) clearance on 1991-02-14. The listed applicant is King Tool, Inc.. The 510(k) number is K905237.

When did EYE SEE INSTRUMENT receive FDA 510(k) clearance?

EYE SEE INSTRUMENT received FDA 510(k) clearance on 1991-02-14, under 510(k) number K905237.

Who is the listed applicant for EYE SEE INSTRUMENT?

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

What is the FDA product code for EYE SEE INSTRUMENT?

The FDA product code for EYE SEE INSTRUMENT is HPN.

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Related Devices (Code: HPN)

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.

K896473H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUREmory University School of MedicineK880855PAREL RARE EARTH MAGNET, I.O.M., INTRAOCULAR MAGRichard James, Inc.K860960RARE EARTH INTRA-OCULAR MAGNETAmeritek, Inc.K831702RARE-EARTH INTRA-OCULAR MAGNETMiami Eye Technology, 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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