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FDA 510(k)

PERIMETRICS PERIOMETER

K-Number: K072213 · 2008-08-29

ApplicantPerimetrics, Inc.
Decision Date2008-08-29
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIMETRICS PERIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Perimetrics, Inc.. It received FDA 510(k) clearance on 2008-08-29 under 510(k) number K072213. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIMETRICS PERIOMETER?

PERIMETRICS PERIOMETER is a medical device that received FDA 510(k) clearance on 2008-08-29. The listed applicant is Perimetrics, Inc.. The 510(k) number is K072213.

When did PERIMETRICS PERIOMETER receive FDA 510(k) clearance?

PERIMETRICS PERIOMETER received FDA 510(k) clearance on 2008-08-29, under 510(k) number K072213.

Who is the listed applicant for PERIMETRICS PERIOMETER?

The FDA 510(k) record lists Perimetrics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERIMETRICS PERIOMETER?

The FDA product code for PERIMETRICS PERIOMETER is EKX.

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 Perimetrics, 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.

K251597InnerView SystemK232657InnerView LC

Related Devices (Code: EKX)

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.

K261987Reusable SmartPegOsstell ABK252223Alpha Endo Handpiece (Alpha Endo)SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.K251597InnerView SystemPerimetrics, Inc.K243692EnDrive (EnDriveUS)Advanced Technology Research (A.T.R.) S.R.L.K242514Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)Shenzhen Rogin Medical Co., Ltd.K241065ChecQ (AC100)Dentis Co., Ltd.

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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