Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PERIO PIK

K-Number: K905188 · 1991-02-15

ApplicantTeledyne Water Pik
Decision Date1991-02-15
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIO PIK 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 1991-02-15 under 510(k) number K905188. 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 PERIO PIK?

PERIO PIK is a medical device that received FDA 510(k) clearance on 1991-02-15. The listed applicant is Teledyne Water Pik. The 510(k) number is K905188.

When did PERIO PIK receive FDA 510(k) clearance?

PERIO PIK received FDA 510(k) clearance on 1991-02-15, under 510(k) number K905188.

Who is the listed applicant for PERIO PIK?

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 PERIO PIK?

The FDA product code for PERIO PIK is EFS.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 SYSTEMK900547WATER PIK(R) W/ADD'L CLAIMS

View all 9 devices →

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.

↑