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FDA 510(k)

WHITE OCULAR PRESSURE RELIEF DEVICE

K-Number: K840204 · 1985-02-15

ApplicantPrecision-Cosmet Co., Inc.
Decision Date1985-02-15
Product CodeKYF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WHITE OCULAR PRESSURE RELIEF DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Precision-Cosmet Co., Inc.. It received FDA 510(k) clearance on 1985-02-15 under 510(k) number K840204. The device is classified under product code KYF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITE OCULAR PRESSURE RELIEF DEVICE?

WHITE OCULAR PRESSURE RELIEF DEVICE is a medical device that received FDA 510(k) clearance on 1985-02-15. The listed applicant is Precision-Cosmet Co., Inc.. The 510(k) number is K840204.

When did WHITE OCULAR PRESSURE RELIEF DEVICE receive FDA 510(k) clearance?

WHITE OCULAR PRESSURE RELIEF DEVICE received FDA 510(k) clearance on 1985-02-15, under 510(k) number K840204.

Who is the listed applicant for WHITE OCULAR PRESSURE RELIEF DEVICE?

The FDA 510(k) record lists Precision-Cosmet Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHITE OCULAR PRESSURE RELIEF DEVICE?

The FDA product code for WHITE OCULAR PRESSURE RELIEF DEVICE is KYF.

Related Clinical Trials

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Other records listing Precision-Cosmet Co., 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.

K861057MANUAL OPHTHALMIC SURGICAL INSTRUMENTSK852934PRECISION - COSMET CAPSULE COUPEURK840104PETRUS IOL GUIDE

Related Devices (Code: KYF)

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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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