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FDA 510(k)

INTRAOCULAR PRESSURE REDUCER

K-Number: K854873 · 1986-02-04

ApplicantMira, Inc.
Decision Date1986-02-04
Product CodeLCR
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

INTRAOCULAR PRESSURE REDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Mira, Inc.. It received FDA 510(k) clearance on 1986-02-04 under 510(k) number K854873. The device is classified under product code LCR. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAOCULAR PRESSURE REDUCER?

INTRAOCULAR PRESSURE REDUCER is a medical device that received FDA 510(k) clearance on 1986-02-04. The listed applicant is Mira, Inc.. The 510(k) number is K854873.

When did INTRAOCULAR PRESSURE REDUCER receive FDA 510(k) clearance?

INTRAOCULAR PRESSURE REDUCER received FDA 510(k) clearance on 1986-02-04, under 510(k) number K854873.

Who is the listed applicant for INTRAOCULAR PRESSURE REDUCER?

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

What is the FDA product code for INTRAOCULAR PRESSURE REDUCER?

The FDA product code for INTRAOCULAR PRESSURE REDUCER is LCR.

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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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