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FDA 510(k)

PRO PULSE PERIODONTAL IRRIGATOR 7618

K-Number: K832222 · 1983-08-31

ApplicantVipont Laboratories, Inc.
Decision Date1983-08-31
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRO PULSE PERIODONTAL IRRIGATOR 7618 is the device name listed in this FDA 510(k) record. The listed applicant is Vipont Laboratories, Inc.. It received FDA 510(k) clearance on 1983-08-31 under 510(k) number K832222. 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 PRO PULSE PERIODONTAL IRRIGATOR 7618?

PRO PULSE PERIODONTAL IRRIGATOR 7618 is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Vipont Laboratories, Inc.. The 510(k) number is K832222.

When did PRO PULSE PERIODONTAL IRRIGATOR 7618 receive FDA 510(k) clearance?

PRO PULSE PERIODONTAL IRRIGATOR 7618 received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832222.

Who is the listed applicant for PRO PULSE PERIODONTAL IRRIGATOR 7618?

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

What is the FDA product code for PRO PULSE PERIODONTAL IRRIGATOR 7618?

The FDA product code for PRO PULSE PERIODONTAL IRRIGATOR 7618 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.

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Other records listing Vipont Laboratories, 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.

K834545POCKETIP 4414K832223PERIODONTAL IRRIGATOR #7620

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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