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FDA 510(k)

KENDRO HERACELL 240 INCUBATOR

K-Number: K023465 · 2003-03-10

Decision Date2003-03-10
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KENDRO HERACELL 240 INCUBATOR is the device name listed in this FDA 510(k) record. The listed applicant is Kendro Laboratory Products, L.P.. It received FDA 510(k) clearance on 2003-03-10 under 510(k) number K023465. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENDRO HERACELL 240 INCUBATOR?

KENDRO HERACELL 240 INCUBATOR is a medical device that received FDA 510(k) clearance on 2003-03-10. The listed applicant is Kendro Laboratory Products, L.P.. The 510(k) number is K023465.

When did KENDRO HERACELL 240 INCUBATOR receive FDA 510(k) clearance?

KENDRO HERACELL 240 INCUBATOR received FDA 510(k) clearance on 2003-03-10, under 510(k) number K023465.

Who is the listed applicant for KENDRO HERACELL 240 INCUBATOR?

The FDA 510(k) record lists Kendro Laboratory Products, L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDRO HERACELL 240 INCUBATOR?

The FDA product code for KENDRO HERACELL 240 INCUBATOR is MQG.

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.

Other records listing Kendro Laboratory Products, L.P. 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.

Related Devices (Code: MQG)

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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