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FDA 510(k)

MILLENNIUM

K-Number: K990908 · 1999-05-27

ApplicantEndo Technic Corp.
Decision Date1999-05-27
Product CodeMXF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MILLENNIUM is the device name listed in this FDA 510(k) record. The listed applicant is Endo Technic Corp.. It received FDA 510(k) clearance on 1999-05-27 under 510(k) number K990908. The device is classified under product code MXF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLENNIUM?

MILLENNIUM is a medical device that received FDA 510(k) clearance on 1999-05-27. The listed applicant is Endo Technic Corp.. The 510(k) number is K990908.

When did MILLENNIUM receive FDA 510(k) clearance?

MILLENNIUM received FDA 510(k) clearance on 1999-05-27, under 510(k) number K990908.

Who is the listed applicant for MILLENNIUM?

The FDA 510(k) record lists Endo Technic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILLENNIUM?

The FDA product code for MILLENNIUM is MXF.

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.

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Other records listing Endo Technic Corp. 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.

K971459DERMALASEK925079LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)K930756LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECEK925114LAPAROSCOPIC INSTRUMENTSK924058TROCARK9148251-125 ENDOSEED

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Related Devices (Code: MXF)

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.

K022803WATERLASE FOR APICOECTOMYBiolase Technology, Inc.K013908WATERLASE MILLENNIUMBiolase Technology, Inc.K012511WATERLASE MILLENNIUMBiolase Technology, Inc.K990219MODIFICATION OF MILLENNIUMBiolase Technology, Inc.

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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