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FDA 510(k)

COMBINATION 6X-MAGNIFIER AND TWEEZERS

K-Number: K896413 · 1990-02-01

ApplicantJames Alexander Corp.
Decision Date1990-02-01
Product CodeLRR
DecisionSubstantially Equivalent

Device Summary

COMBINATION 6X-MAGNIFIER AND TWEEZERS is the device name listed in this FDA 510(k) record. The listed applicant is James Alexander Corp.. It received FDA 510(k) clearance on 1990-02-01 under 510(k) number K896413. The device is classified under product code LRR. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMBINATION 6X-MAGNIFIER AND TWEEZERS?

COMBINATION 6X-MAGNIFIER AND TWEEZERS is a medical device that received FDA 510(k) clearance on 1990-02-01. The listed applicant is James Alexander Corp.. The 510(k) number is K896413.

When did COMBINATION 6X-MAGNIFIER AND TWEEZERS receive FDA 510(k) clearance?

COMBINATION 6X-MAGNIFIER AND TWEEZERS received FDA 510(k) clearance on 1990-02-01, under 510(k) number K896413.

Who is the listed applicant for COMBINATION 6X-MAGNIFIER AND TWEEZERS?

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

What is the FDA product code for COMBINATION 6X-MAGNIFIER AND TWEEZERS?

The FDA product code for COMBINATION 6X-MAGNIFIER AND TWEEZERS is LRR.

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Related Devices (Code: LRR)

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Official Source

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