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FDA 510(k)

DENTAL SYRINGE SYSTEM-VARIOUS STYLES

K-Number: K832662 · 1983-10-04

ApplicantCentrix, Inc.
Decision Date1983-10-04
Product CodeKXR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL SYRINGE SYSTEM-VARIOUS STYLES is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832662. The device is classified under product code KXR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL SYRINGE SYSTEM-VARIOUS STYLES?

DENTAL SYRINGE SYSTEM-VARIOUS STYLES is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Centrix, Inc.. The 510(k) number is K832662.

When did DENTAL SYRINGE SYSTEM-VARIOUS STYLES receive FDA 510(k) clearance?

DENTAL SYRINGE SYSTEM-VARIOUS STYLES received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832662.

Who is the listed applicant for DENTAL SYRINGE SYSTEM-VARIOUS STYLES?

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

What is the FDA product code for DENTAL SYRINGE SYSTEM-VARIOUS STYLES?

The FDA product code for DENTAL SYRINGE SYSTEM-VARIOUS STYLES is KXR.

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.

Other records listing Centrix, 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.

View all 46 devices →

Related Devices (Code: KXR)

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.

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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