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FDA 510(k)

ARIOL

K-Number: K033200 · 2004-03-18

ApplicantApplied Imaging Corp.
Decision Date2004-03-18
Product CodeNQN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ARIOL is the device name listed in this FDA 510(k) record. The listed applicant is Applied Imaging Corp.. It received FDA 510(k) clearance on 2004-03-18 under 510(k) number K033200. The device is classified under product code NQN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARIOL?

ARIOL is a medical device that received FDA 510(k) clearance on 2004-03-18. The listed applicant is Applied Imaging Corp.. The 510(k) number is K033200.

When did ARIOL receive FDA 510(k) clearance?

ARIOL received FDA 510(k) clearance on 2004-03-18, under 510(k) number K033200.

Who is the listed applicant for ARIOL?

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

What is the FDA product code for ARIOL?

The FDA product code for ARIOL is NQN.

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Other records listing Applied Imaging 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.

K043519ARIOL HER-2/NEU FISHK042542CYTOVISION FOR CEP XYK031715ARIOL HER-2/NEU IHCK001420SLIDESCANK980375WINSCAN AUTOMATED IMAGING SYSTEMK902311GENEVISION - COMPUTER ASSISTED CHROMOSOME KARYO.

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Related Devices (Code: NQN)

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K130515VIRTUOSO SYSTEM FOR IHC ER (SPI)Ventana Medical Systems, Inc.K121516VIRTUOSO SYSTEM FOR IHC HER2 (4B5)Ventana Medical Systems, Inc.K122143VIRTUOSO SYSTEM FOR IHC PR (1E2) BENCHMARK ULTRA STAINERVentana Medical Systems, Inc.K111872VIRTUOSO SYSTEM FOR IHC P53 (DO-7)Ventana Medical Systems, Inc.K111869VIRTUOSO SYSTEM FOR IHC PR (IE2)Ventana Medical Systems, Inc.K092333PATHIAM SYSTEM WITH ISCAN FOR P53 AND KI-67Bioimagene, 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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