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FDA 510(k)

PERIODONTAL IRRIGATOR #7620

K-Number: K832223 · 1983-08-31

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

Device Summary

PERIODONTAL IRRIGATOR #7620 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 K832223. 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 PERIODONTAL IRRIGATOR #7620?

PERIODONTAL IRRIGATOR #7620 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 K832223.

When did PERIODONTAL IRRIGATOR #7620 receive FDA 510(k) clearance?

PERIODONTAL IRRIGATOR #7620 received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832223.

Who is the listed applicant for PERIODONTAL IRRIGATOR #7620?

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 PERIODONTAL IRRIGATOR #7620?

The FDA product code for PERIODONTAL IRRIGATOR #7620 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 4414K832222PRO PULSE PERIODONTAL IRRIGATOR 7618

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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