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FDA 510(k)

HEAL FORCE CO2 INCUBATOR

K-Number: K101988 · 2011-02-08

Decision Date2011-02-08
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HEAL FORCE CO2 INCUBATOR is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Lishen Scientific Equipment Co., Ltd.. It received FDA 510(k) clearance on 2011-02-08 under 510(k) number K101988. 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 HEAL FORCE CO2 INCUBATOR?

HEAL FORCE CO2 INCUBATOR is a medical device that received FDA 510(k) clearance on 2011-02-08. The listed applicant is Shanghai Lishen Scientific Equipment Co., Ltd.. The 510(k) number is K101988.

When did HEAL FORCE CO2 INCUBATOR receive FDA 510(k) clearance?

HEAL FORCE CO2 INCUBATOR received FDA 510(k) clearance on 2011-02-08, under 510(k) number K101988.

Who is the listed applicant for HEAL FORCE CO2 INCUBATOR?

The FDA 510(k) record lists Shanghai Lishen Scientific Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEAL FORCE CO2 INCUBATOR?

The FDA product code for HEAL FORCE CO2 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.

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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