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FDA 510(k)

NUNC IVF MULTIDISH 4 WELLS NUNCLON

K-Number: K040717 · 2004-08-12

ApplicantNunc A/S
Decision Date2004-08-12
Product CodeMQK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NUNC IVF MULTIDISH 4 WELLS NUNCLON is the device name listed in this FDA 510(k) record. The listed applicant is Nunc A/S. It received FDA 510(k) clearance on 2004-08-12 under 510(k) number K040717. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUNC IVF MULTIDISH 4 WELLS NUNCLON?

NUNC IVF MULTIDISH 4 WELLS NUNCLON is a medical device that received FDA 510(k) clearance on 2004-08-12. The listed applicant is Nunc A/S. The 510(k) number is K040717.

When did NUNC IVF MULTIDISH 4 WELLS NUNCLON receive FDA 510(k) clearance?

NUNC IVF MULTIDISH 4 WELLS NUNCLON received FDA 510(k) clearance on 2004-08-12, under 510(k) number K040717.

Who is the listed applicant for NUNC IVF MULTIDISH 4 WELLS NUNCLON?

The FDA 510(k) record lists Nunc A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NUNC IVF MULTIDISH 4 WELLS NUNCLON?

The FDA product code for NUNC IVF MULTIDISH 4 WELLS NUNCLON is MQK.

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.

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Other records listing Nunc A/S 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.

K070047NUNC IVF DISHES AND NUNC IVF 4-WELL DISH

Related Devices (Code: MQK)

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

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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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