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FDA 510(k)

INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM

K-Number: K883719 · 1988-10-18

ApplicantBiophysic Medical, Inc.
Decision Date1988-10-18
Product CodeLQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biophysic Medical, Inc.. It received FDA 510(k) clearance on 1988-10-18 under 510(k) number K883719. 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 INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM?

INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM is a medical device that received FDA 510(k) clearance on 1988-10-18. The listed applicant is Biophysic Medical, Inc.. The 510(k) number is K883719.

When did INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM receive FDA 510(k) clearance?

INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM received FDA 510(k) clearance on 1988-10-18, under 510(k) number K883719.

Who is the listed applicant for INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM?

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

What is the FDA product code for INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM?

The FDA product code for INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM is LQJ.

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Other records listing Biophysic Medical, 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.

K953399NEEDLE OR CUTTERK893035OPHTHASCAN 'S' MINI-AK890509INDIRECT OPHTHALMOSCOPE ACCESSORY DELIVERY SYSTEMK884595OPHTHASCAN MINI-BK884456STERILE DISPOSABLE ENDOCULAR PROBEK881494FOUR MODIFICATIONS TO OPHTHALAS ARGON/DYE LASER

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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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