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FDA 510(k)

ORAVIEW BY WATER PIK

K-Number: K800919 · 1980-05-08

ApplicantTeledyne, Inc.
Decision Date1980-05-08
Product CodeEAX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORAVIEW BY WATER PIK is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne, Inc.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800919. The device is classified under product code EAX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORAVIEW BY WATER PIK?

ORAVIEW BY WATER PIK is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Teledyne, Inc.. The 510(k) number is K800919.

When did ORAVIEW BY WATER PIK receive FDA 510(k) clearance?

ORAVIEW BY WATER PIK received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800919.

Who is the listed applicant for ORAVIEW BY WATER PIK?

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

What is the FDA product code for ORAVIEW BY WATER PIK?

The FDA product code for ORAVIEW BY WATER PIK is EAX.

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Other records listing Teledyne, 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.

K871828TED MODEL 760K863131PIK POCKET (IRRIGATING TIP)K862695FLUOR-ETCH GEL ETCHANTK854817INSTAPUREK840721PERIO PIKK810864WATER PIK ORAL HYGIENE CENTER

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Related Devices (Code: EAX)

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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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