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FDA 510(k)

PLASMA ARC CURING SYSTEM

K-Number: K952333 · 1995-08-10

ApplicantAmerican Dental Technologies, Inc.
Decision Date1995-08-10
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLASMA ARC CURING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is American Dental Technologies, Inc.. It received FDA 510(k) clearance on 1995-08-10 under 510(k) number K952333. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASMA ARC CURING SYSTEM?

PLASMA ARC CURING SYSTEM is a medical device that received FDA 510(k) clearance on 1995-08-10. The listed applicant is American Dental Technologies, Inc.. The 510(k) number is K952333.

When did PLASMA ARC CURING SYSTEM receive FDA 510(k) clearance?

PLASMA ARC CURING SYSTEM received FDA 510(k) clearance on 1995-08-10, under 510(k) number K952333.

Who is the listed applicant for PLASMA ARC CURING SYSTEM?

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

What is the FDA product code for PLASMA ARC CURING SYSTEM?

The FDA product code for PLASMA ARC CURING SYSTEM is EBF.

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Other records listing American Dental Technologies, 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.

K023547DIOLASE 980 D LASER SYSTEMK012127PULSEMASTER ERBIUM DENTAL LASER SYSTEMK012213GULLIVER AND CLASSE AK984486PULSEMASTER DENTAL LASER SYSTEMK972325PULSEMASTER 1000 ST DENTAL LASER SYSTEMK961269PULSEMASTER

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, Inc.

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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