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FDA 510(k)

SHARPLAN LASER POSITIONING SYSTEM

K-Number: K837573 · 1983-06-28

ApplicantLaser Industries , Ltd.
Decision Date1983-06-28
Product Code
DecisionSubstantially Equivalent

Device Summary

SHARPLAN LASER POSITIONING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Laser Industries , Ltd.. It received FDA 510(k) clearance on 1983-06-28 under 510(k) number K837573. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPLAN LASER POSITIONING SYSTEM?

SHARPLAN LASER POSITIONING SYSTEM is a medical device that received FDA 510(k) clearance on 1983-06-28. The listed applicant is Laser Industries , Ltd.. The 510(k) number is K837573.

When did SHARPLAN LASER POSITIONING SYSTEM receive FDA 510(k) clearance?

SHARPLAN LASER POSITIONING SYSTEM received FDA 510(k) clearance on 1983-06-28, under 510(k) number K837573.

Who is the listed applicant for SHARPLAN LASER POSITIONING SYSTEM?

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

Related Clinical Trials

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Other records listing Laser Industries , Ltd. 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.

K933362SHARPLAN CO2 SURGICAL LASERK894765SHARPLAN SMOKE EVACUATION UNIT, MODEL 100K850633SHARPLAN MODEL 1060 CO/2 SURGICAL LASERK850628SHARPLAN 1040 CO/2 SURGICAL LASERK842997LASER RECTOSCOPE SET 784K832550SHARPLAN #734 LASER SURGICAL UNIT

View all 20 devices →

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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