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FDA 510(k)

SLIDESCAN

K-Number: K001420 · 2000-08-30

ApplicantApplied Imaging Corp.
Decision Date2000-08-30
Product CodeJOY
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SLIDESCAN 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 2000-08-30 under 510(k) number K001420. The device is classified under product code JOY. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIDESCAN?

SLIDESCAN is a medical device that received FDA 510(k) clearance on 2000-08-30. The listed applicant is Applied Imaging Corp.. The 510(k) number is K001420.

When did SLIDESCAN receive FDA 510(k) clearance?

SLIDESCAN received FDA 510(k) clearance on 2000-08-30, under 510(k) number K001420.

Who is the listed applicant for SLIDESCAN?

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 SLIDESCAN?

The FDA product code for SLIDESCAN is JOY.

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Other records listing Applied Imaging Corp. as applicant

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K043519ARIOL HER-2/NEU FISHK042542CYTOVISION FOR CEP XYK033200ARIOLK031715ARIOL HER-2/NEU IHCK980375WINSCAN AUTOMATED IMAGING SYSTEMK902311GENEVISION - COMPUTER ASSISTED CHROMOSOME KARYO.

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Related Devices (Code: JOY)

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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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