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FDA 510(k)

CENTRIX RIBBON TUBES

K-Number: K853282 · 1985-08-23

ApplicantCentrix, Inc.
Decision Date1985-08-23
Product CodeEID
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CENTRIX RIBBON TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1985-08-23 under 510(k) number K853282. The device is classified under product code EID. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIX RIBBON TUBES?

CENTRIX RIBBON TUBES is a medical device that received FDA 510(k) clearance on 1985-08-23. The listed applicant is Centrix, Inc.. The 510(k) number is K853282.

When did CENTRIX RIBBON TUBES receive FDA 510(k) clearance?

CENTRIX RIBBON TUBES received FDA 510(k) clearance on 1985-08-23, under 510(k) number K853282.

Who is the listed applicant for CENTRIX RIBBON TUBES?

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 CENTRIX RIBBON TUBES?

The FDA product code for CENTRIX RIBBON TUBES is EID.

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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.

K250714FluoroDose VarnishK222459Centrix FluoroSilver Silver Diamine Fluoride 38%K152826NoCordK120176SENZZZZZ AWAYK111348RE / STASIS (TM) GINGIVAL RETRACTION PASTEK092384LIQUICORD

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Related Devices (Code: EID)

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.

K941431BONE GRAFT DELIVERY SYRINGESBio-Interfaces, Inc.K913974ACCESS IMPRESSION BARRELCentrix, Inc.K873153CAULK'S VPS CARTRIDGE SYSTEMDentsply Intl.K871937IMPRESSION SYRINGEDentsply Intl.K863998COLTENE JET-MIXERColtene, Inc.K851386UNITEK DISPOSABLE IMPRESSION SYRINGEUnitek Corp.

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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