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FDA 510(k)

PREVIEW XT

K-Number: K854282 · 1986-01-08

ApplicantCambridge Medical Instruments, Inc.
Decision Date1986-01-08
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PREVIEW XT is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Medical Instruments, Inc.. It received FDA 510(k) clearance on 1986-01-08 under 510(k) number K854282. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREVIEW XT?

PREVIEW XT is a medical device that received FDA 510(k) clearance on 1986-01-08. The listed applicant is Cambridge Medical Instruments, Inc.. The 510(k) number is K854282.

When did PREVIEW XT receive FDA 510(k) clearance?

PREVIEW XT received FDA 510(k) clearance on 1986-01-08, under 510(k) number K854282.

Who is the listed applicant for PREVIEW XT?

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

What is the FDA product code for PREVIEW XT?

The FDA product code for PREVIEW XT is DSI.

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Other records listing Cambridge Medical Instruments, Inc. as applicant

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Related Devices (Code: DSI)

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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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