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FDA 510(k)

INTERJET(TM) GINGIVAL CARE INSTRUMENT

K-Number: K921999 · 1992-06-03

ApplicantBausch & Lomb, Inc.
Decision Date1992-06-03
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERJET(TM) GINGIVAL CARE INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 1992-06-03 under 510(k) number K921999. 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 INTERJET(TM) GINGIVAL CARE INSTRUMENT?

INTERJET(TM) GINGIVAL CARE INSTRUMENT is a medical device that received FDA 510(k) clearance on 1992-06-03. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K921999.

When did INTERJET(TM) GINGIVAL CARE INSTRUMENT receive FDA 510(k) clearance?

INTERJET(TM) GINGIVAL CARE INSTRUMENT received FDA 510(k) clearance on 1992-06-03, under 510(k) number K921999.

Who is the listed applicant for INTERJET(TM) GINGIVAL CARE INSTRUMENT?

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

What is the FDA product code for INTERJET(TM) GINGIVAL CARE INSTRUMENT?

The FDA product code for INTERJET(TM) GINGIVAL CARE INSTRUMENT is EFS.

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Other records listing Bausch & Lomb, 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.

K192005Bausch + Lomb PreVue Inserter for enVista PreloadedK173480Crystalsert Lens Delivery SystemK161012Easy-Load Lens Delivery SystemK131208BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,K122575BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VIK113852BAUSCH & LOMB IOL INJECTOR

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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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