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FDA 510(k)

CRADLE PACS

K-Number: K033912 · 2004-05-11

ApplicantCradle Technology Corp.
Decision Date2004-05-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CRADLE PACS is the device name listed in this FDA 510(k) record. The listed applicant is Cradle Technology Corp.. It received FDA 510(k) clearance on 2004-05-11 under 510(k) number K033912. 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 CRADLE PACS?

CRADLE PACS is a medical device that received FDA 510(k) clearance on 2004-05-11. The listed applicant is Cradle Technology Corp.. The 510(k) number is K033912.

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

CRADLE PACS received FDA 510(k) clearance on 2004-05-11, under 510(k) number K033912.

Who is the listed applicant for CRADLE PACS?

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

What is the FDA product code for CRADLE PACS?

The FDA product code for CRADLE 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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