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FDA 510(k)

CROUCH CORNEAL PROTECTOR

K-Number: K833256 · 1984-02-08

ApplicantStar Instrument Co.
Decision Date1984-02-08
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CROUCH CORNEAL PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Star Instrument Co.. It received FDA 510(k) clearance on 1984-02-08 under 510(k) number K833256. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROUCH CORNEAL PROTECTOR?

CROUCH CORNEAL PROTECTOR is a medical device that received FDA 510(k) clearance on 1984-02-08. The listed applicant is Star Instrument Co.. The 510(k) number is K833256.

When did CROUCH CORNEAL PROTECTOR receive FDA 510(k) clearance?

CROUCH CORNEAL PROTECTOR received FDA 510(k) clearance on 1984-02-08, under 510(k) number K833256.

Who is the listed applicant for CROUCH CORNEAL PROTECTOR?

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

What is the FDA product code for CROUCH CORNEAL PROTECTOR?

The FDA product code for CROUCH CORNEAL PROTECTOR is HOY.

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Related Devices (Code: HOY)

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Official Source

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

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