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FDA 510(k)

BRILLETTE MODEL

K-Number: K842835 · 1984-11-21

ApplicantCillus Company, Inc.
Decision Date1984-11-21
Product CodeHOI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BRILLETTE MODEL is the device name listed in this FDA 510(k) record. The listed applicant is Cillus Company, Inc.. It received FDA 510(k) clearance on 1984-11-21 under 510(k) number K842835. The device is classified under product code HOI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRILLETTE MODEL?

BRILLETTE MODEL is a medical device that received FDA 510(k) clearance on 1984-11-21. The listed applicant is Cillus Company, Inc.. The 510(k) number is K842835.

When did BRILLETTE MODEL receive FDA 510(k) clearance?

BRILLETTE MODEL received FDA 510(k) clearance on 1984-11-21, under 510(k) number K842835.

Who is the listed applicant for BRILLETTE MODEL?

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

What is the FDA product code for BRILLETTE MODEL?

The FDA product code for BRILLETTE MODEL is HOI.

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Related Devices (Code: HOI)

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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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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