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FDA 510(k)

MODEL 716 MICROMANIPULATOR

K-Number: K828056 · 1983-01-06

ApplicantLaser Industries , Ltd.
Decision Date1983-01-06
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL 716 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 1983-01-06 under 510(k) number K828056. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 716 MICROMANIPULATOR?

MODEL 716 MICROMANIPULATOR is a medical device that received FDA 510(k) clearance on 1983-01-06. The listed applicant is Laser Industries , Ltd.. The 510(k) number is K828056.

When did MODEL 716 MICROMANIPULATOR receive FDA 510(k) clearance?

MODEL 716 MICROMANIPULATOR received FDA 510(k) clearance on 1983-01-06, under 510(k) number K828056.

Who is the listed applicant for MODEL 716 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 100K850633SHARPLAN MODEL 1060 CO/2 SURGICAL LASERK850628SHARPLAN 1040 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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