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FDA 510(k)

WATER PIK PLUS PLAQUE CONTROL SYSTEM

K-Number: K931380 · 1993-09-20

ApplicantTeledyne Water Pik
Decision Date1993-09-20
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WATER PIK PLUS PLAQUE CONTROL SYSTEM 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 1993-09-20 under 510(k) number K931380. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATER PIK PLUS PLAQUE CONTROL SYSTEM?

WATER PIK PLUS PLAQUE CONTROL SYSTEM is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Teledyne Water Pik. The 510(k) number is K931380.

When did WATER PIK PLUS PLAQUE CONTROL SYSTEM receive FDA 510(k) clearance?

WATER PIK PLUS PLAQUE CONTROL SYSTEM received FDA 510(k) clearance on 1993-09-20, under 510(k) number K931380.

Who is the listed applicant for WATER PIK PLUS PLAQUE CONTROL SYSTEM?

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 PLUS PLAQUE CONTROL SYSTEM?

The FDA product code for WATER PIK PLUS PLAQUE CONTROL SYSTEM is EFS.

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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 SYSTEMK940288WATER PIK SENSONIC PLAQUE REMOVAL INSTRUMENTK905188PERIO PIKK900547WATER PIK(R) W/ADD'L CLAIMS

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Related Devices (Code: EFS)

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.

K023232SPLATRFREE SWANGLE 360 DISPOSABLE PROPHYLAXIS ANGLESmartpracticeK001493DENTAL AIR FORCE HOME DENTAL CLEANING SYSTEM, MODEL NO. 0020001Air Force, Inc.K983374AGATHA-A-H2010Midian Intl.K964810DERMADAMUltradent Products, Inc.K952234BARRIER ALL FILMCottrell, Ltd.K943182ORAL-B PERIOFLEX SUBGINGIVAL IRRIGATOROral-B Laboratories

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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