DENTAL SYRINGE SYSTEM-VARIOUS STYLES
K-Number: K832662 · 1983-10-04
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Device Summary
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.
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
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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