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FDA 510(k)

LASER CENTERING DEVICE

K-Number: K872747 · 1987-09-04

ApplicantInnomed Corp.
Decision Date1987-09-04
Product CodeHMR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LASER CENTERING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Innomed Corp.. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K872747. The device is classified under product code HMR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER CENTERING DEVICE?

LASER CENTERING DEVICE is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is Innomed Corp.. The 510(k) number is K872747.

When did LASER CENTERING DEVICE receive FDA 510(k) clearance?

LASER CENTERING DEVICE received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872747.

Who is the listed applicant for LASER CENTERING DEVICE?

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

What is the FDA product code for LASER CENTERING DEVICE?

The FDA product code for LASER CENTERING DEVICE is HMR.

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 Innomed 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.

K822574INNOMED PD-1 KITK827796INNOSCAN EXAMINATION LIGHT

Related Devices (Code: HMR)

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.

K053475OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-450Refractec, Inc.K925606OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERSChiron Vision Corp.K863663OPHTHALMIC SURGICAL OCULAR MARKERSMyocure, Inc.K861535OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNUCooperVision, 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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