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FDA 510(k)

OPHTHALMIC TRICHIASIS PROBE

K-Number: K923629 · 1992-10-19

ApplicantMira, Inc.
Decision Date1992-10-19
Product CodeHPS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC TRICHIASIS PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Mira, Inc.. It received FDA 510(k) clearance on 1992-10-19 under 510(k) number K923629. The device is classified under product code HPS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALMIC TRICHIASIS PROBE?

OPHTHALMIC TRICHIASIS PROBE is a medical device that received FDA 510(k) clearance on 1992-10-19. The listed applicant is Mira, Inc.. The 510(k) number is K923629.

When did OPHTHALMIC TRICHIASIS PROBE receive FDA 510(k) clearance?

OPHTHALMIC TRICHIASIS PROBE received FDA 510(k) clearance on 1992-10-19, under 510(k) number K923629.

Who is the listed applicant for OPHTHALMIC TRICHIASIS PROBE?

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 OPHTHALMIC TRICHIASIS PROBE?

The FDA product code for OPHTHALMIC TRICHIASIS PROBE is HPS.

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Other records listing Mira, Inc. as applicant

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Related Devices (Code: HPS)

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K202038CryoTreQVitreQ BVK940373OPHTHALMIC CRYO UNITDutch Ophthalmic USA, Inc.K903303SPEMBLY MEDICAL 242 CRYOUNIT/SERIES 242 CRYOPROBESSpembly Medical , Ltd.K874555KEELER ACU 22XT OPHTHALMIC CRYO UNITKeeler Instruments, Inc.K873388KEELER CTU CRYO SYSTEMKeeler Instruments, Inc.K870195UNITED SURGICAL CORP. CRYOPTIC PLUSUnited Surgical Corp.

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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