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FDA 510(k)

CENTAURI

K-Number: K905141 · 1991-02-11

ApplicantPfizer Laser Systems
Decision Date1991-02-11
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CENTAURI is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer Laser Systems. It received FDA 510(k) clearance on 1991-02-11 under 510(k) number K905141. 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 CENTAURI?

CENTAURI is a medical device that received FDA 510(k) clearance on 1991-02-11. The listed applicant is Pfizer Laser Systems. The 510(k) number is K905141.

When did CENTAURI receive FDA 510(k) clearance?

CENTAURI received FDA 510(k) clearance on 1991-02-11, under 510(k) number K905141.

Who is the listed applicant for CENTAURI?

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

What is the FDA product code for CENTAURI?

The FDA product code for CENTAURI is HQF.

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Other records listing Pfizer Laser Systems 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.

K910826ORION YAG LASER SYSTEM OPHTHALMOLOGYK911288ORIONK910825ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC.K912067POLARIS, GYNECOLOGY INDICATIONSK910152ORIONK912813SIRIUS

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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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