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FDA 510(k)

EXEL 1800 AND 1800E CT SCANNER

K-Number: K884670 · 1989-01-18

ApplicantElscint, Inc.
Decision Date1989-01-18
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EXEL 1800 AND 1800E CT SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1989-01-18 under 510(k) number K884670. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXEL 1800 AND 1800E CT SCANNER?

EXEL 1800 AND 1800E CT SCANNER is a medical device that received FDA 510(k) clearance on 1989-01-18. The listed applicant is Elscint, Inc.. The 510(k) number is K884670.

When did EXEL 1800 AND 1800E CT SCANNER receive FDA 510(k) clearance?

EXEL 1800 AND 1800E CT SCANNER received FDA 510(k) clearance on 1989-01-18, under 510(k) number K884670.

Who is the listed applicant for EXEL 1800 AND 1800E CT SCANNER?

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

What is the FDA product code for EXEL 1800 AND 1800E CT SCANNER?

The FDA product code for EXEL 1800 AND 1800E CT SCANNER is JAK.

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Other records listing Elscint, Inc. as applicant

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Related Devices (Code: JAK)

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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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