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FDA 510(k)

CHILI PACS

K-Number: K070796 · 2007-04-06

ApplicantChili GmbH
Decision Date2007-04-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CHILI PACS is the device name listed in this FDA 510(k) record. The listed applicant is Chili GmbH. It received FDA 510(k) clearance on 2007-04-06 under 510(k) number K070796. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHILI PACS?

CHILI PACS is a medical device that received FDA 510(k) clearance on 2007-04-06. The listed applicant is Chili GmbH. The 510(k) number is K070796.

When did CHILI PACS receive FDA 510(k) clearance?

CHILI PACS received FDA 510(k) clearance on 2007-04-06, under 510(k) number K070796.

Who is the listed applicant for CHILI PACS?

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

What is the FDA product code for CHILI PACS?

The FDA product code for CHILI PACS is LLZ.

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Related Devices (Code: LLZ)

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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