FDA 510(k)

23:1 REDUCTION ANGLE

K-Number: K973800 · 1998-03-11

Decision Date1998-03-11

Product CodeEGS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

23:1 REDUCTION ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Dental Products Corp.. It received FDA 510(k) clearance on 1998-03-11 under 510(k) number K973800. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 23:1 REDUCTION ANGLE?

23:1 REDUCTION ANGLE is a medical device that received FDA 510(k) clearance on 1998-03-11. The listed applicant is Midwest Dental Products Corp.. The 510(k) number is K973800.

When did 23:1 REDUCTION ANGLE receive FDA 510(k) clearance?

23:1 REDUCTION ANGLE received FDA 510(k) clearance on 1998-03-11, under 510(k) number K973800.

Who is the listed applicant for 23:1 REDUCTION ANGLE?

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

What is the FDA product code for 23:1 REDUCTION ANGLE?

The FDA product code for 23:1 REDUCTION ANGLE is EGS.

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Other records listing Midwest Dental Products Corp. as applicant

K964755MICROJET CAVITY PREPARATION SYSTEM K962877MIDWEST 300 SE K963050TRADITION P, PUSH BUTTON HANDPIECE K955655MIDWEST ONE

Related Devices (Code: EGS)

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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.