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FDA 510(k)

LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1

K-Number: K871245 · 1987-05-07

ApplicantChiron Vision Corp.
Decision Date1987-05-07
Product CodeLQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1 is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1987-05-07 under 510(k) number K871245. 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 LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1?

LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1 is a medical device that received FDA 510(k) clearance on 1987-05-07. The listed applicant is Chiron Vision Corp.. The 510(k) number is K871245.

When did LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1 receive FDA 510(k) clearance?

LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1 received FDA 510(k) clearance on 1987-05-07, under 510(k) number K871245.

Who is the listed applicant for LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1?

The FDA 510(k) record lists Chiron Vision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1?

The FDA product code for LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1 is LQJ.

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Other records listing Chiron Vision Corp. 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.

K970727MPORT FOLDABLE LENS PLACEMENT SYSTEMK972808HANSATOME MICROKERATOMEK960414SYNERGIST POWER PACKK944993IOLAB.SITE CD PHACOEMULSIFICATION MODULEK944995IOLAB/SITE PERISTALTIC MODULEK951292PASSPORT FOLDABLE LENS PLACEMENT SYSTEM

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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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