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FDA 510(k)

PETRUS SINGLE MIRROR LASER LENS

K-Number: K862869 · 1986-08-21

ApplicantOcular Instruments, Inc.
Decision Date1986-08-21
Product CodeLQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PETRUS SINGLE MIRROR LASER 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 1986-08-21 under 510(k) number K862869. The device is classified under product code LQJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PETRUS SINGLE MIRROR LASER LENS?

PETRUS SINGLE MIRROR LASER LENS is a medical device that received FDA 510(k) clearance on 1986-08-21. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K862869.

When did PETRUS SINGLE MIRROR LASER LENS receive FDA 510(k) clearance?

PETRUS SINGLE MIRROR LASER LENS received FDA 510(k) clearance on 1986-08-21, under 510(k) number K862869.

Who is the listed applicant for PETRUS SINGLE MIRROR LASER 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 PETRUS SINGLE MIRROR LASER LENS?

The FDA product code for PETRUS SINGLE MIRROR LASER LENS is LQJ.

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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: LQJ)

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.

K163632Katalyst Cyclophotocoagulation ProbeKatalyst Surgical, LLCK931356SAFE AIR VARI-SPOT HANDPIECE TELESCOPE AND ADAPTORSorenson Laboratories, Inc.K921414TROKEL /3 GONIO LASER LENSOcular Instruments, Inc.K912112PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480Tomey Corporation USAK893731SHIELDS T.C. LASER LENSOcular Instruments, Inc.K884694MQL 20 ND:YAG OPHTHALMIC LASERCalifornia Laboratories, Inc.

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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