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FDA 510(k)

SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M

K-Number: K013703 · 2001-12-14

ApplicantSanyo North America Corp.
Decision Date2001-12-14
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M is the device name listed in this FDA 510(k) record. The listed applicant is Sanyo North America Corp.. It received FDA 510(k) clearance on 2001-12-14 under 510(k) number K013703. 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 SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M?

SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M is a medical device that received FDA 510(k) clearance on 2001-12-14. The listed applicant is Sanyo North America Corp.. The 510(k) number is K013703.

When did SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M receive FDA 510(k) clearance?

SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M received FDA 510(k) clearance on 2001-12-14, under 510(k) number K013703.

Who is the listed applicant for SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M?

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

What is the FDA product code for SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M?

The FDA product code for SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M is MQG.

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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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