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FDA 510(k)

MIN-IDENTOFLEX

K-Number: K873002 · 1987-08-17

ApplicantCentrix, Inc.
Decision Date1987-08-17
Product CodeEHJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIN-IDENTOFLEX is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1987-08-17 under 510(k) number K873002. The device is classified under product code EHJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIN-IDENTOFLEX?

MIN-IDENTOFLEX is a medical device that received FDA 510(k) clearance on 1987-08-17. The listed applicant is Centrix, Inc.. The 510(k) number is K873002.

When did MIN-IDENTOFLEX receive FDA 510(k) clearance?

MIN-IDENTOFLEX received FDA 510(k) clearance on 1987-08-17, under 510(k) number K873002.

Who is the listed applicant for MIN-IDENTOFLEX?

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 MIN-IDENTOFLEX?

The FDA product code for MIN-IDENTOFLEX is EHJ.

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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: EHJ)

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.

K911111MICROMILLS, PATRIOTS, ALPHA GOLD DIAMONDSVermont Diamond InstrumentsK790640HOWMEDICA BRASS CENTER DISCE.C. Moore Co.K771658IDENTOFLEXCavitron 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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