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FDA 510(k)

W&H 900 INCOLIGHT LT HANDPIECE

K-Number: K944718 · 1995-10-05

ApplicantA-Dec, Inc.
Decision Date1995-10-05
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

W&H 900 INCOLIGHT LT HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is A-Dec, Inc.. It received FDA 510(k) clearance on 1995-10-05 under 510(k) number K944718. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the W&H 900 INCOLIGHT LT HANDPIECE?

W&H 900 INCOLIGHT LT HANDPIECE is a medical device that received FDA 510(k) clearance on 1995-10-05. The listed applicant is A-Dec, Inc.. The 510(k) number is K944718.

When did W&H 900 INCOLIGHT LT HANDPIECE receive FDA 510(k) clearance?

W&H 900 INCOLIGHT LT HANDPIECE received FDA 510(k) clearance on 1995-10-05, under 510(k) number K944718.

Who is the listed applicant for W&H 900 INCOLIGHT LT HANDPIECE?

The FDA 510(k) record lists A-Dec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for W&H 900 INCOLIGHT LT HANDPIECE?

The FDA product code for W&H 900 INCOLIGHT LT HANDPIECE is EFB.

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Other records listing A-Dec, 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.

K213932A-dec 300, A-dec 500K102234A-DEC 200 DENTAL SYSTEMK100647A-DEC/W&H SYNEA SONIC SCALER HANDPIECE, MODELS ZA-55, ZA-55 L, ZA-55 LM, ZA-55M, SF1LMK082716A-DEC/W&H ALEGRA AIR-DRIVEN HIGHSPEED HANDPIECE, MODEL TE-97, TE-98, A-DEC/W&H ALEGRA HANDPIECE ATTACHMENT, MODEL HE-43K082827A-DEC/W&H PROFIN RECIPROCATING CONTRA-ANGLE HANDPIECE ATTACHMENTK082985A-DEC 334/335 DELIVERY SYSTEM

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Related Devices (Code: EFB)

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.

K262144DIAMED Handpiece;DIAMED Airmotor;DIAMED Airmotor HandpieceSETAGAYA SEIKI Co., Ltd.K251388Dental air-motor handpiece (TM-203B2, TM-203M4, TM-205B2, TM-205M4, TM-IS, TM-ES, TM-SG20, TM-X25, TM-BB, TM-IC, TM-RA41)Foshan Topmed Dental Co., Ltd.K251389High speed air turbine handpieceFoshan Topmed Dental Co., Ltd.K242179Synea Fusion Handpieces (Intensiv & Profin)W&H Dentalwerk Bürmoos GmbHK240337Dental Handpiece (Model: J6-126, J6-136, SH11W2, SH11W3, W401LW, W15LW, W142LW, W11L)Guangdong Jinme Medical Technology Co., Ltd.K241074High-speed Air Turbine Handpieces (SCHG01, SCHG03, SCHG18, SCHF19, SCHF22), Dental Low Speed Handpieces including Straight and Geared Angle Handpieces and Air Motors (Straight Handpieces: SCHD05-S, SCHD16-S, SCHD17-S, SCHD24-S, SCHD27-S Geared Angle Handpieces: SCHD05-C, SCHD06-C, SCHD16-C, SCHD17-C, SCHD24-C, SCHD27-C, SCHD29-S, SCHB4, SCHB5, SCHB20, SCHB64 Air Motors: SCHD16-M, SCHD17-M, SCHD24-M, SCHD27-M)Foshan Soco Precision Instrument Co., Ltd.

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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