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FDA 510(k)

BYRNE EXPULSIVE LENS

K-Number: K923670 · 1992-11-16

ApplicantOcular Instruments, Inc.
Decision Date1992-11-16
Product CodeHJI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BYRNE EXPULSIVE LENS is the device name listed in this FDA 510(k) record. The listed applicant is Ocular Instruments, Inc.. It received FDA 510(k) clearance on 1992-11-16 under 510(k) number K923670. The device is classified under product code HJI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BYRNE EXPULSIVE LENS?

BYRNE EXPULSIVE LENS is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K923670.

When did BYRNE EXPULSIVE LENS receive FDA 510(k) clearance?

BYRNE EXPULSIVE LENS received FDA 510(k) clearance on 1992-11-16, under 510(k) number K923670.

Who is the listed applicant for BYRNE EXPULSIVE LENS?

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

What is the FDA product code for BYRNE EXPULSIVE LENS?

The FDA product code for BYRNE EXPULSIVE LENS is HJI.

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Other records listing Ocular Instruments, 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.

K014170STAURENGHI WIDE FIELD SCANNING LASER LENSK012096DISPOSABLE VITRECTOMY LENSK933976MANDELKORN SUTURE LYSIS LENSK933264RITCH NYLON SUTURE LASER LENSK94142050 DEGREE HRI PRISM LENSK935302OSHER SURGICAL GONIO/POSTERIOR POLE LENS

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Related Devices (Code: HJI)

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.

K902138STRIPE PROJECTORAcademic Catalyst Corp.K90183960 FUNDUS CAMERA CF-60UVCanon USA, Inc.K897186LASER IMAGING WORK STATIONInnovision Medical, Inc.K820223OMS QUARTZ INFUSION CONTACT LENSOptical Micro Systems, Inc.K802971LANDERS CONTACT LENSCooper Medical Devices Corp.K802927SEBESTYEN IRRIGATING CONTACT LENSCooper Medical Devices 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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