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FDA 510(k)

BQ/BM INTEGRATED LASER DELIVERY SYSTEM

K-Number: K990665 · 1999-05-17

ApplicantAmerican Laser Corp.
Decision Date1999-05-17
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BQ/BM INTEGRATED LASER DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is American Laser Corp.. It received FDA 510(k) clearance on 1999-05-17 under 510(k) number K990665. 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 BQ/BM INTEGRATED LASER DELIVERY SYSTEM?

BQ/BM INTEGRATED LASER DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-05-17. The listed applicant is American Laser Corp.. The 510(k) number is K990665.

When did BQ/BM INTEGRATED LASER DELIVERY SYSTEM receive FDA 510(k) clearance?

BQ/BM INTEGRATED LASER DELIVERY SYSTEM received FDA 510(k) clearance on 1999-05-17, under 510(k) number K990665.

Who is the listed applicant for BQ/BM INTEGRATED LASER DELIVERY SYSTEM?

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

What is the FDA product code for BQ/BM INTEGRATED LASER DELIVERY SYSTEM?

The FDA product code for BQ/BM INTEGRATED LASER DELIVERY SYSTEM is HQF.

Related Clinical Trials

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.

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Other records listing American Laser 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.

K010046NUVOLASE 532 MEDICAL LASER SYSTEMK990725NUVOLASE 532 LASER SYSTEMK827819LASER PHOTOCOAGULATORK813429LASER PHOTOCOAGULATOR ARGON MED. 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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