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FDA 510(k)

MODEL 900K PHOTOCOAGULATOR

K-Number: K801336 · 1980-07-28

ApplicantCoherent Medical Division
Decision Date1980-07-28
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODEL 900K PHOTOCOAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Coherent Medical Division. It received FDA 510(k) clearance on 1980-07-28 under 510(k) number K801336. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 900K PHOTOCOAGULATOR?

MODEL 900K PHOTOCOAGULATOR is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Coherent Medical Division. The 510(k) number is K801336.

When did MODEL 900K PHOTOCOAGULATOR receive FDA 510(k) clearance?

MODEL 900K PHOTOCOAGULATOR received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801336.

Who is the listed applicant for MODEL 900K PHOTOCOAGULATOR?

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

What is the FDA product code for MODEL 900K PHOTOCOAGULATOR?

The FDA product code for MODEL 900K PHOTOCOAGULATOR is HQF.

Related Clinical Trials

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Other records listing Coherent Medical Division 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.

K902990COHERENT HOLMIUM:YAG SURGICAL LASERK822908COHERENT FUNDUSL RETINAL CAMERAK822415THE OCUPLOT DK801906DIOPTRON III AUTOREFRACTORK791895ACCESSORIES FOR SYS. 400 CO2 SURG. LASER

Related Devices (Code: HQF)

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.

K252979Voyager DSLT (430840610)Belkin Vision, Ltd.K251507INTEGRE LIOQuantel MedicalK251772Navilas Laser System 577sl (156691)Od-Os GmbHK243014EyeQ nanoECPEyeq, Inc.K240615Leos Laser and Endoscopy SystemBeaver-Visitec International, Inc.K242397LYNX PhotocoagulatorNorlase Aps

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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