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FDA 510(k)

MODEL 712 MICROMANIPULATOR

K-Number: K827607 · 1982-07-22

ApplicantLaser Industries , Ltd.
Decision Date1982-07-22
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL 712 MICROMANIPULATOR 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 1982-07-22 under 510(k) number K827607. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 712 MICROMANIPULATOR?

MODEL 712 MICROMANIPULATOR is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Laser Industries , Ltd.. The 510(k) number is K827607.

When did MODEL 712 MICROMANIPULATOR receive FDA 510(k) clearance?

MODEL 712 MICROMANIPULATOR received FDA 510(k) clearance on 1982-07-22, under 510(k) number K827607.

Who is the listed applicant for MODEL 712 MICROMANIPULATOR?

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

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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 100K850628SHARPLAN 1040 CO/2 SURGICAL LASERK850633SHARPLAN MODEL 1060 CO/2 SURGICAL LASERK842997LASER RECTOSCOPE SET 784K832550SHARPLAN #734 LASER SURGICAL UNIT

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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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