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FDA 510(k)

ACCESS IMPRESSION BARREL

K-Number: K913974 · 1992-02-25

ApplicantCentrix, Inc.
Decision Date1992-02-25
Product CodeEID
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCESS IMPRESSION BARREL is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1992-02-25 under 510(k) number K913974. 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 ACCESS IMPRESSION BARREL?

ACCESS IMPRESSION BARREL is a medical device that received FDA 510(k) clearance on 1992-02-25. The listed applicant is Centrix, Inc.. The 510(k) number is K913974.

When did ACCESS IMPRESSION BARREL receive FDA 510(k) clearance?

ACCESS IMPRESSION BARREL received FDA 510(k) clearance on 1992-02-25, under 510(k) number K913974.

Who is the listed applicant for ACCESS IMPRESSION BARREL?

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 ACCESS IMPRESSION BARREL?

The FDA product code for ACCESS IMPRESSION BARREL 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.K873153CAULK'S VPS CARTRIDGE SYSTEMDentsply Intl.K871937IMPRESSION SYRINGEDentsply Intl.K863998COLTENE JET-MIXERColtene, Inc.K853282CENTRIX RIBBON TUBESCentrix, 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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