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FDA 510(k)

PIK POCKET(R), MODEL PP-3

K-Number: K895259 · 1989-11-01

ApplicantTeledyne Water Pik
Decision Date1989-11-01
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PIK POCKET(R), MODEL PP-3 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 1989-11-01 under 510(k) number K895259. 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 PIK POCKET(R), MODEL PP-3?

PIK POCKET(R), MODEL PP-3 is a medical device that received FDA 510(k) clearance on 1989-11-01. The listed applicant is Teledyne Water Pik. The 510(k) number is K895259.

When did PIK POCKET(R), MODEL PP-3 receive FDA 510(k) clearance?

PIK POCKET(R), MODEL PP-3 received FDA 510(k) clearance on 1989-11-01, under 510(k) number K895259.

Who is the listed applicant for PIK POCKET(R), MODEL PP-3?

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 PIK POCKET(R), MODEL PP-3?

The FDA product code for PIK POCKET(R), MODEL PP-3 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 INSTRUMENTK931380WATER PIK PLUS PLAQUE CONTROL SYSTEMK905188PERIO PIK

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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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