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FDA 510(k)

ILLUMINATOR

K-Number: K954787 · 1996-01-31

ApplicantHospitak, Inc.
Decision Date1996-01-31
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1996-01-31 under 510(k) number K954787. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILLUMINATOR?

ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1996-01-31. The listed applicant is Hospitak, Inc.. The 510(k) number is K954787.

When did ILLUMINATOR receive FDA 510(k) clearance?

ILLUMINATOR received FDA 510(k) clearance on 1996-01-31, under 510(k) number K954787.

Who is the listed applicant for ILLUMINATOR?

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

What is the FDA product code for ILLUMINATOR?

The FDA product code for ILLUMINATOR is CCW.

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Other records listing Hospitak, 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.

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Related Devices (Code: CCW)

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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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