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FDA 510(k)

APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR

K-Number: K883904 · 1988-12-07

ApplicantApollo Dental Products, Inc.
Decision Date1988-12-07
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR is the device name listed in this FDA 510(k) record. The listed applicant is Apollo Dental Products, Inc.. It received FDA 510(k) clearance on 1988-12-07 under 510(k) number K883904. 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 APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR?

APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR is a medical device that received FDA 510(k) clearance on 1988-12-07. The listed applicant is Apollo Dental Products, Inc.. The 510(k) number is K883904.

When did APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR receive FDA 510(k) clearance?

APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR received FDA 510(k) clearance on 1988-12-07, under 510(k) number K883904.

Who is the listed applicant for APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR?

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

What is the FDA product code for APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR?

The FDA product code for APOLLO VS, VT, VR 1000/1500, FREEDOM HS, HT, HR is EIA.

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.

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Other records listing Apollo Dental Products, 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.

K852816FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10

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

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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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