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FDA 510(k)

SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR

K-Number: K913848 · 1992-03-27

Decision Date1992-03-27
Product CodeMGI
DecisionSubstantially Equivalent

Device Summary

SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Sharplan Lasers, Inc.. It received FDA 510(k) clearance on 1992-03-27 under 510(k) number K913848. The device is classified under product code MGI. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR?

SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR is a medical device that received FDA 510(k) clearance on 1992-03-27. The listed applicant is Sharplan Lasers, Inc.. The 510(k) number is K913848.

When did SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR receive FDA 510(k) clearance?

SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR received FDA 510(k) clearance on 1992-03-27, under 510(k) number K913848.

Who is the listed applicant for SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR?

The FDA 510(k) record lists Sharplan Lasers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR?

The FDA product code for SHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATOR is MGI.

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.

Other records listing Sharplan Lasers, Inc. 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.

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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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