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FDA 510(k)

EVACUATOR, ORAL CAVITY

K-Number: K932824 · 1993-09-28

ApplicantDen-Tal-Ez Mfg Co., Inc.
Decision Date1993-09-28
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EVACUATOR, ORAL CAVITY is the device name listed in this FDA 510(k) record. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. It received FDA 510(k) clearance on 1993-09-28 under 510(k) number K932824. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVACUATOR, ORAL CAVITY?

EVACUATOR, ORAL CAVITY is a medical device that received FDA 510(k) clearance on 1993-09-28. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. The 510(k) number is K932824.

When did EVACUATOR, ORAL CAVITY receive FDA 510(k) clearance?

EVACUATOR, ORAL CAVITY received FDA 510(k) clearance on 1993-09-28, under 510(k) number K932824.

Who is the listed applicant for EVACUATOR, ORAL CAVITY?

The FDA 510(k) record lists Den-Tal-Ez Mfg Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVACUATOR, ORAL CAVITY?

The FDA product code for EVACUATOR, ORAL CAVITY is EIA.

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Other records listing Den-Tal-Ez Mfg Co., Inc. as applicant

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Related Devices (Code: EIA)

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.

K251544Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)Lakong Medical Devices Co., Ltd.K251626Midmark Dental Delivery SystemMidmark CorporationK251491K5 Cart, K5 Mount, K5 SwingOsstem Implant Company., Ltd. Chair BusinessK243130Integral Dental UnitGuangdong Yadeng Medical Apparatus Co., Ltd.,K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd.K250473Dental Delivery System Series 5 and Dental Delivery System Series 5 PlusDci International, LLC

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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