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FDA 510(k)

WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT

K-Number: K940288 · 1994-05-26

ApplicantTeledyne Water Pik
Decision Date1994-05-26
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Water Pik. It received FDA 510(k) clearance on 1994-05-26 under 510(k) number K940288. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT?

WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1994-05-26. The listed applicant is Teledyne Water Pik. The 510(k) number is K940288.

When did WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT receive FDA 510(k) clearance?

WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT received FDA 510(k) clearance on 1994-05-26, under 510(k) number K940288.

Who is the listed applicant for WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT?

The FDA 510(k) record lists Teledyne Water Pik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT?

The FDA product code for WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENT is JEQ.

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Other records listing Teledyne Water Pik 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.

K970594KALGINATE IMPRESSION MATERIALK952422ELASTIC IMPRESSION CREAMK944162DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEMK931380WATER PIK PLUS PLAQUE CONTROL SYSTEMK905188PERIO PIKK900547WATER PIK(R) W/ADD'L CLAIMS

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Related Devices (Code: JEQ)

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.

K200881Oral-B iO Test Drive Power Brush Trial Program KitThe Procter & Gamble CompanyK061351ORAL-B SONIC COMPLETEBraun GmbHK061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESBraun GmbHK040416SONICARE ADVANCE TOOTHBRUSH, MODEL 4900Philips Oral Healthcare, Inc.K022900BUTLER GUM VARI-CLEAN POWER TOOTHBRUSHESJohn O. Butler Co.K012914SONICWAVE SONIC PLAQUE REMOVERHomedics, 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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