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FDA 510(k)

COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS

K-Number: K060316 · 2006-06-23

Decision Date2006-06-23
Product CodeLZH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius Kabi Deutschland GmbH. It received FDA 510(k) clearance on 2006-06-23 under 510(k) number K060316. The device is classified under product code LZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS?

COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS is a medical device that received FDA 510(k) clearance on 2006-06-23. The listed applicant is Fresenius Kabi Deutschland GmbH. The 510(k) number is K060316.

When did COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS receive FDA 510(k) clearance?

COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS received FDA 510(k) clearance on 2006-06-23, under 510(k) number K060316.

Who is the listed applicant for COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS?

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

What is the FDA product code for COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS?

The FDA product code for COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS is LZH.

Related Clinical Trials

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.

Related Devices (Code: LZH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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