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FDA 510(k)

PHOTOCOAGULATOR LASER

K-Number: K780345 · 1978-05-09

ApplicantCavitron Corp.
Decision Date1978-05-09
Product CodeHQB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHOTOCOAGULATOR LASER is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1978-05-09 under 510(k) number K780345. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTOCOAGULATOR LASER?

PHOTOCOAGULATOR LASER is a medical device that received FDA 510(k) clearance on 1978-05-09. The listed applicant is Cavitron Corp.. The 510(k) number is K780345.

When did PHOTOCOAGULATOR LASER receive FDA 510(k) clearance?

PHOTOCOAGULATOR LASER received FDA 510(k) clearance on 1978-05-09, under 510(k) number K780345.

Who is the listed applicant for PHOTOCOAGULATOR LASER?

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

What is the FDA product code for PHOTOCOAGULATOR LASER?

The FDA product code for PHOTOCOAGULATOR LASER is HQB.

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Other records listing Cavitron 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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Related Devices (Code: HQB)

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.

K220263Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical ChandeliersVortex Surgical, Inc.K191846MAXReach Laser ProbeVortex Surgical, Inc.K182646Vitreq disposable laser probes, light fibers and ChandelierVitreQ BVK132614PEREGRINE CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K12299723GA CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K122905PEREGRINE 23GA CURVED LASER PROBEPeregrine Surgical , Ltd.

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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